CClinicalTrials.gg
CompletedNCT00535938Updated Sep 10, 2014Results posted

MDs on Botox Utility (MOBILITY)

An observational study in Blepharospasm, Torticollis and Strabismus, sponsored by Allergan. Completed at 1 site in Canada. Open to participants aged 14 Years and older. Per ClinicalTrials.gov, last updated 2014-09-10.

Sponsored by Allergan · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
1,372
Ages
14 Years and older
Sex
All
01

Study summary

The MOBILITY Project is a prospective, non-randomized, observational, multi-centre evaluation of Health Utility via the SF-12® Health Survey Scores and the SF-6D in patients receiving BOTOX® for therapeutic use.

02

Conditions studied

  • Blepharospasm
  • Torticollis
  • Strabismus
  • Muscle Spasticity
03

Who can participate

Ages eligible
14 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Community sample

Inclusion criteria

  • Patients who are eligible for BOTOX® treatment deemed medically necessary by their physician
  • Patient (and/or patient's authorized legal representative) should provide written informed consent; a patient under the age of 18 must review and sign the Patient Assent Form
  • Patients at the age of or over 14

Exclusion criteria

Exclusion Criteria:

  • Patient is participating in a clinical trial for any BOTOX® indication
  • Patient with any contraindications to use botulinum toxin A
04

Study design

Time perspective
Prospective
Enrollment
1,372 participants (actual)

Groups and cohorts

  • Naïve to Botox® treatment

    Initiating treatment with BOTOX® upon entry to the project.

    Other: botulinum toxin type A

  • Non-naïve to Botox® treatment

    Receiving ongoing treatment with BOTOX® upon entry to the project.

    Other: botulinum toxin type A

Interventions

  • Otherbotulinum toxin type A

    There will be no protocol-mandated intervention with regard to physician treatment choice or management of patient condition once the patient is enrolled in the project.

05

What researchers measure

Primary outcomes

  1. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cervical Dystonia

    Cervical dystonia is a condition in which the neck muscles contract involuntarily, causing the head to turn to one side, forward or backward. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 505 days for patients with cervical dystonia.

    Time frame: Baseline, SV1 (up to 505 days)

  2. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Blepharospasm

    Blepharospasm is a condition in which the eyelids blink/close involuntarily. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 542 days for patients with blepharospasm.

    Time frame: Baseline, SV1 (up to 542 days)

  3. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Hyperhidrosis

    Hyperhidrosis is a condition causing excessive sweating, regardless of temperature or exercise. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,273 days for patients with hyperhidrosis.

    Time frame: Baseline, SV1 (up to 1,273 days)

  4. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cerebral Palsy

    Cerebral Palsy is a disability resulting in muscular incoordination and speech disturbances. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 925 days for patients with cerebral palsy.

    Time frame: Baseline, SV1 (up to 925 days)

  5. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Adult Focal Spasticity

    Adult Focal Spasticity is a condition in which muscles are continuously tight or stiff in a certain area. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,562 days for patients with adult focal spasticity.

    Time frame: Baseline, SV1 (up to 1,562 days)

  6. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Facial Nerve Disorder

    Facial nerve disorder is a condition causing twitching, weakness or paralysis of the face. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 765 days for patients with facial nerve disorder.

    Time frame: Baseline, SV1 (up to 765 days)

  7. Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With "Other" Disorders

    "Other" disorders include focal dystonia (involuntary muscular contractions/abnormal postures), headache, pain, tics (sudden, repetitive, nonrhythmic movements/vocalizations), tremors (unintentional, rhythmic muscle movements), and other nonspecified disorders. The SF-12 is 12 questions on various health questions. Health utility is a numerical indicator of a person's preference for a given health state or health outcome. Health utility is a sub-score ranging from 0(death) to 1(perfect health) calculated from the SF-12 total score based on: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and SV1 is scheduled at the physician's discretion and was a maximum of 568 days for patients with "other" disorders.

    Time frame: Baseline, SV1 (up to 568 days)

Secondary outcomes

  1. BOTOX® Dose in Patients With Cervical Dystonia

    Cervical dystonia is a condition in which the neck muscles contract involuntarily, causing the head to turn to one side, forward or backward. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 505 days for patients with cervical dystonia.

    Time frame: Baseline, SV1 (up to 505 days)

  2. BOTOX® Dose in Patients With Blepharospasm

    Blepharospasm is a condition in which the eyelids blink/close involuntarily. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 542 days for patients with blepharospasm.

    Time frame: Baseline, SV1 (up to 542 days)

  3. BOTOX® Dose in Patients With Hyperhidrosis

    Hyperhidrosis is a condition causing excessive sweating, regardless of temperature or exercise. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,273 days for patients with hyperhidrosis.

    Time frame: Baseline, SV1 (up to 1,273 days)

  4. BOTOX® Dose in Patients With Adult Focal Spasticity

    Adult Focal Spasticity is a condition in which muscles are continuously tight or stiff in a certain area. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,562 days for patients with adult focal spasticity.

    Time frame: Baseline, SV1 (up to 1,562 days)

  5. BOTOX® Dose in Patients With Cerebral Palsy

    Cerebral Palsy is a disability resulting in muscular incoordination and speech disturbances. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 925 days for patients with cerebral palsy.

    Time frame: Baseline, SV1 (up to 925 days)

  6. BOTOX® Dose in Patients With Facial Nerve Disorder

    Facial nerve disorder is a condition causing twitching, weakness or paralysis of the face. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 765 days for patients with facial nerve disorder.

    Time frame: Baseline, SV1 (up to 765 days)

  7. BOTOX® Dose in Patients With "Other" Disorders

    "Other" disorders include focal dystonia (involuntary muscular contractions/abnormal postures), headache, pain, tics (sudden, repetitive, nonrhythmic movements/vocalizations), tremors (unintentional, rhythmic muscle movements), and other nonspecified disorders. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 568 days for patients with "other" disorders.

    Time frame: Baseline, SV1 (up to 568 days)

  8. Concurrent Procedure Resource Utilization Patterns

    Resource utilization patterns are assessed in terms of concurrent procedures utilized during the study (up to 1,785 days across all indications) and are grouped by highest level term. (Note: NEC=not elsewhere classified)

    Time frame: Up to 1,785 days

  9. Concurrent Surgical Procedure Resource Utilization Patterns

    Resource utilization patterns are assessed in terms of concurrent surgical procedures utilized during the study (up to 1,785 days across all indications) and are grouped by highest level term. (Note: NEC=not elsewhere classified)

    Time frame: Up to 1,785 days

06

Results

Posted Sep 10, 2014

Participant flow

Participant flow — Overall Study
MilestoneNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Started506866
Completed115404
Not completed391462

Outcome measures

PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cervical Dystonia

Cervical dystonia is a condition in which the neck muscles contract involuntarily, causing the head to turn to one side, forward or backward. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 505 days for patients with cervical dystonia.

Time frame:
Baseline, SV1 (up to 505 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cervical Dystonia
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.650 ± 0.1540.676 ± 0.143
Change from Baseline at SV1 (N=33,174)0.020 ± 0.084-0.001 ± 0.104
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Blepharospasm

Blepharospasm is a condition in which the eyelids blink/close involuntarily. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 542 days for patients with blepharospasm.

Time frame:
Baseline, SV1 (up to 542 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Blepharospasm
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.718 ± 0.1220.754 ± 0.132
Change from Baseline at SV1 (N=21, 51)0.053 ± 0.1560.014 ± 0.120
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Hyperhidrosis

Hyperhidrosis is a condition causing excessive sweating, regardless of temperature or exercise. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,273 days for patients with hyperhidrosis.

Time frame:
Baseline, SV1 (up to 1,273 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Hyperhidrosis
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.782 ± 0.1290.799 ± 0.115
Change from Baseline at SV1 (N=58, 60)0.010 ± 0.136-0.000 ± 0.124
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cerebral Palsy

Cerebral Palsy is a disability resulting in muscular incoordination and speech disturbances. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 925 days for patients with cerebral palsy.

Time frame:
Baseline, SV1 (up to 925 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Cerebral Palsy
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.712 ± 0.1310.733 ± 0.117
Change from Baseline at SV1 (N=0, 8)NA ± NA0.018 ± 0.114
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Adult Focal Spasticity

Adult Focal Spasticity is a condition in which muscles are continuously tight or stiff in a certain area. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,562 days for patients with adult focal spasticity.

Time frame:
Baseline, SV1 (up to 1,562 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Adult Focal Spasticity
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.621 ± 0.1110.635 ± 0.124
Change from Baseline at Week 4 (N=114, 201)0.002 ± 0.0960.008 ± 0.096
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Facial Nerve Disorder

Facial nerve disorder is a condition causing twitching, weakness or paralysis of the face. The SF-12 consists of 12 questions on various health questions. Health utility is a numerical indicator of a person's preferences for a given health state or health outcome. Health utility is a sub-score ranging from 0 (death) to 1 (perfect health) and is calculated from the SF-12 total score based on the following items: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 765 days for patients with facial nerve disorder.

Time frame:
Baseline, SV1 (up to 765 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With Facial Nerve Disorder
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.770 ± 0.1340.759 ± 0.134
Change from Baseline at SV1 (N=30, 63)0.035 ± 0.1580.002 ± 0.111
PrimaryChange From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With "Other" Disorders

"Other" disorders include focal dystonia (involuntary muscular contractions/abnormal postures), headache, pain, tics (sudden, repetitive, nonrhythmic movements/vocalizations), tremors (unintentional, rhythmic muscle movements), and other nonspecified disorders. The SF-12 is 12 questions on various health questions. Health utility is a numerical indicator of a person's preference for a given health state or health outcome. Health utility is a sub-score ranging from 0(death) to 1(perfect health) calculated from the SF-12 total score based on: physical functioning, role participation, social functioning, bodily pain, mental health, and vitality and is termed SF-6D. A positive change from baseline indicates an improvement and a negative change from baseline indicates a worsening. The length of time between Baseline and SV1 is scheduled at the physician's discretion and was a maximum of 568 days for patients with "other" disorders.

Time frame:
Baseline, SV1 (up to 568 days)
Reported as:
Mean · Scores on a Scale
Change From Baseline in the SF-6D Measure Health Utility (Quality of Life) Score Using the SF-12® Questionnaire for Patients With "Other" Disorders
Scores on a ScaleNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline0.570 ± 0.1370.610 ± 0.118
Change from Baseline at SV1 (N=33, 72)0.060 ± 0.0860.028 ± 0.113
SecondaryBOTOX® Dose in Patients With Cervical Dystonia

Cervical dystonia is a condition in which the neck muscles contract involuntarily, causing the head to turn to one side, forward or backward. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 505 days for patients with cervical dystonia.

Time frame:
Baseline, SV1 (up to 505 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Cervical Dystonia
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline154.8 ± 61.1242.7 ± 99.6
SV1 (N=37, 187)169.9 ± 70.2246.4 ± 101.7
SecondaryBOTOX® Dose in Patients With Blepharospasm

Blepharospasm is a condition in which the eyelids blink/close involuntarily. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 542 days for patients with blepharospasm.

Time frame:
Baseline, SV1 (up to 542 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Blepharospasm
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline42.9 ± 13.867.3 ± 54.3
SV1 (N=23, 54)47.8 ± 22.761.9 ± 39.5
SecondaryBOTOX® Dose in Patients With Hyperhidrosis

Hyperhidrosis is a condition causing excessive sweating, regardless of temperature or exercise. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,273 days for patients with hyperhidrosis.

Time frame:
Baseline, SV1 (up to 1,273 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Hyperhidrosis
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline192.5 ± 60.4203.6 ± 74.8
SV1 (N=80, 97)186.9 ± 53.8206.5 ± 81.6
SecondaryBOTOX® Dose in Patients With Adult Focal Spasticity

Adult Focal Spasticity is a condition in which muscles are continuously tight or stiff in a certain area. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 1,562 days for patients with adult focal spasticity.

Time frame:
Baseline, SV1 (up to 1,562 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Adult Focal Spasticity
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline253.0 ± 132.6346.4 ± 157.4
SV1 (N=127, 225)295.4 ± 152.4355.8 ± 150.2
SecondaryBOTOX® Dose in Patients With Cerebral Palsy

Cerebral Palsy is a disability resulting in muscular incoordination and speech disturbances. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 925 days for patients with cerebral palsy.

Time frame:
Baseline, SV1 (up to 925 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Cerebral Palsy
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline260.0 ± 89.4245.5 ± 101.1
SV1 (N=1, 12)200.0 ± NA252.5 ± 105.2
SecondaryBOTOX® Dose in Patients With Facial Nerve Disorder

Facial nerve disorder is a condition causing twitching, weakness or paralysis of the face. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 765 days for patients with facial nerve disorder.

Time frame:
Baseline, SV1 (up to 765 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With Facial Nerve Disorder
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline31.3 ± 13.740.6 ± 25.4
SV1 (N=31, 69)30.9 ± 13.444.1 ± 31.2
SecondaryBOTOX® Dose in Patients With "Other" Disorders

"Other" disorders include focal dystonia (involuntary muscular contractions/abnormal postures), headache, pain, tics (sudden, repetitive, nonrhythmic movements/vocalizations), tremors (unintentional, rhythmic muscle movements), and other nonspecified disorders. The BOTOX® dose was assessed in this patient population. The length of time between Baseline and Subsequent Visit 1 (SV1) is scheduled at the physician's discretion and was a maximum of 568 days for patients with "other" disorders.

Time frame:
Baseline, SV1 (up to 568 days)
Reported as:
Mean · Units
BOTOX® Dose in Patients With "Other" Disorders
UnitsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Baseline157.2 ± 82.4187.2 ± 106.8
SV1 (N=40, 75)173.4 ± 106.9185.7 ± 110.1
SecondaryConcurrent Procedure Resource Utilization Patterns

Resource utilization patterns are assessed in terms of concurrent procedures utilized during the study (up to 1,785 days across all indications) and are grouped by highest level term. (Note: NEC=not elsewhere classified)

Time frame:
Up to 1,785 days
Reported as:
Number · Patients
Concurrent Procedure Resource Utilization Patterns
PatientsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Bone and joint therapeutic procedures03
Economic and housing issues21
Eye therapeutic procedures10
Lifestyle issues39
Therapeutic procedures and supportive care NEC4169
SecondaryConcurrent Surgical Procedure Resource Utilization Patterns

Resource utilization patterns are assessed in terms of concurrent surgical procedures utilized during the study (up to 1,785 days across all indications) and are grouped by highest level term. (Note: NEC=not elsewhere classified)

Time frame:
Up to 1,785 days
Reported as:
Number · Patients
Concurrent Surgical Procedure Resource Utilization Patterns
PatientsNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
Bone and joint therapeutic procedures26
Eye therapeutic procedures12
Gastrointestinal therapeutic procedures01
Head and neck therapeutic procedures01
Nervous system, skull&spine therapeutic procedures26
Renal/urinary tract investigations & urinalyses10
Renal and urinary tract therapeutic procedures01
Skin appendage conditions01
Soft tissue therapeutic procedures26
Therapeutic procedures and supportive care NEC11
Vascular therapeutic procedures01

Adverse events

Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Naïve to Botox® Treatment—5/506 (1%)0/506 (0%)
Non-naïve to Botox® Treatment—33/866 (3.8%)0/866 (0%)
Most frequent serious events
Showing 10 of 53
Most frequent serious events
EventNaïve to Botox® TreatmentNon-naïve to Botox® Treatment
DeathGeneral disorders1/5066/866
DysphagiaGastrointestinal disorders1/5064/866
AstheniaGeneral disorders0/5062/866
Hip FractureInjury, poisoning and procedural complications1/5062/866
Myocardial InfarctionCardiac disorders0/5062/866
Small Intestinal ObstructionGastrointestinal disorders0/5062/866
DepressionPsychiatric disorders0/5062/866
Foot DeformityMusculoskeletal and connective tissue disorders1/5060/866
Multiple SclerosisNervous system disorders1/5060/866
Neoplasm MalignantNeoplasms benign, malignant and unspecified (incl cysts and polyps)1/5060/866

Baseline characteristics

Age, Customized
Age, Customized(Participants)Naïve to Botox® TreatmentNon-naïve to Botox® TreatmentTotal
14 to 17 years222850
18 to 65 years3746411015
>65 years110197307
Sex: Female, Male
Sex: Female, Male(Participants)Naïve to Botox® TreatmentNon-naïve to Botox® TreatmentTotal
Female304577881
Male202289491
07

Study locations

1 site
  • Toronto, Ontario, Canada
08

Registry details

Key details

Study ID
NCT00535938
Lead sponsor
Allergan
Responsible party
Sponsor
First posted
Sep 27, 2007
Start date
Sep 2007
Primary completion
Sep 2013
Completion
Sep 2013
Results posted
Sep 10, 2014
Last update
Sep 10, 2014

Study contacts

Medical Director
study director · Allergan

Oversight

Data monitoring committee
No
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Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

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