CClinicalTrials.gg
CompletedNCT01018264URGE-PDUpdated Nov 9, 2021Results posted

Solifenacin Succinate (VESIcare) for the Treatment of Overactive Bladder in Parkinson's Disease

A Phase 4 interventional study of solifenacin succinate (VESIcare) and placebo in Overactive Bladder in Parkinson's Disease, sponsored by University of South Florida. Completed at 3 sites in United States. Open to participants aged 40 Years to 80 Years. Per ClinicalTrials.gov, last updated 2021-11-09.

Sponsored by University of South Florida · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
23
Allocation
Randomized
Ages
40 Years to 80 Years
Sex
All
01

Study summary

This study will assess the effectiveness of solifenacin succinate (VESIcare) in reducing symptoms of overactive bladder in Parkinson's disease (PD) patients.

02

Conditions studied

  • Overactive Bladder in Parkinson's Disease

Keywords

  • Overactive bladder
  • Urinary incontinence
  • Urinary frequency
  • Parkinson's disease
03

In context

Parkinson Disease

4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.

This study's enrollment of 23 is below the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

University of South Florida is the lead sponsor of 333 studies on the registry; 63 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 4 (24%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Outpatients with idiopathic PD according to the UK Parkinson's Disease Society Brain Bank Clinical Diagnosis Criteria.
  2. Age 40 years to 80 years.
  3. Stable dose of antiparkinsonian medication 4 weeks prior to study entry.
  4. Patients must score 1.0 to 3.0 on the Modified Hoehn and Yahr scale.
  5. Women of child-bearing potential must use a reliable method of contraception.
  6. Must be experiencing symptoms of overactive bladder according to the ICS definition of a minimum voiding 8 or more times/24 hours and a daily average of at least 1 episode of urgency and/or urinary incontinence (urge incontinence predominately as measured by 3IQ diary) per 24 hours during a 3-day micturition diary period. Patients must have documentation of OAB within the last 6 months.
  7. The patient must have evidence of PSA less than or equal to 4 (males only) within the last 12 months (obtained from primary care physician).
  8. The patient must have had a bladder scan within six months of the screening visit. This scan uses ultrasound technology to measure residual fluid levels in the bladder after urination. This scan must document post void residual of 200 mls or less. A bladder scan printout or a note documenting these findings must be provided before baseline.
  9. Clearance from the patient's internist or primary care health provider who has examined the patient within the last 6 months.

Exclusion criteria

Exclusion Criteria:

  1. Any illness that in the investigator's opinion preclude participation in this study.
  2. Pregnancy or lactation.
  3. Concurrent participation in another clinical study.
  4. Dementia or other psychiatric illness that prevents the patient from giving informed consent (Mini Mental Status Exam scores less than 27).
  5. Legal incapacity or limited legal capacity.
  6. History of prostate cancer or Transurethral resection of the prostate (TURP) (males only).
  7. Presence of severe renal disease. BUN 50% greater than normal (normal BUN levels should be within a range of 5 to 20 mg/ d L and creatinine between .7 and 1.4 mg/ d L). Labs within the past 12 months will be requested from the patient's health care provider or urologist. If labs are not available within this time-frame or if results are abnormal, labs will be obtained as part of the screening visit.
  8. Presence of major hepatic impairment (cirrhosis, viral hepatitis, nonalcoholic steatohepatitis, Wilson's disease, or Hemochromotosis).
  9. Currently taking ketaconazole (anti-fungal) or any CYP3A4 inhibitor such as itraconazole, ritonavir, nelfinavir, clarithromycin, or nefazadone.
  10. Any history of bladder outflow obstruction or gastrointestinal obstructive disorders.
  11. History of narrow angle glaucoma.
  12. Patients who have undergone pelvic radiation at any time.
  13. Currently taking any of the following medications:

    • Antiarrhythmics: flecainide (Almarytm, Apocard, Ecrinal, Flécaine), digoxin (Lanoxin, Digitek, Lanoxicaps)
    • Antipsychotics: thioridazine (Mellaril, Novorizadine, Thioril)
    • Tricyclic anti-depressants: amitriptyline (Elavil, Tryptanol, Endep, Elatrol, Tryptizol, Trepiline, Laroxyl), amoxapine (Asendin, Asendis, Defanyl, Demolox, Moxadil), clomipramine (Anafranil), desipramine (Norpramin, Pertofrane), imipramine (Antideprin, Deprenil, Deprimin, Deprinol, Depsonil, Dynaprin, Eupramin, Imipramil, Irmin, Janimine, Melipramin, Surplix, Tofranil), nortriptyline (Aventyl, Pamelor, Nortrilen), protriptyline (Vivactil), trimipramine (Stangyl, Surmontil, Rhotrimine)
    • Psychotropics: doxepin (Aponal, Adapine, Sinquan, Sinequan)
    • Anticholinergics/Antispasmodics: trihexyphenidyl (Artane, Aparkan), benztropine (Cogentin), oxybutynin (Ditropan, Ditropan XL, Lyrinel XL, Oxytrol), darifenacin (Enablex), emepronium, flavoxate (Urispas), meladrazine, propiverine, solifenacin (Vesicare), tolterodine (Detrol, Detrol LA), trospium (Sanctura)
    • Selective Serotonin-Norepinephrine Reuptake Inhibitors (SNRI): duloxetine (Cymbalta, Yentreve), Venlafaxine (Effexor, Effexor XR)
    • Arylalkylamines: pseudoephedrine (Sudafed)
    • Anti-androgen: bicalutamide (Casodex, Cosudex, Calutide, Kalumid), finasteride (Proscar, Propecia, Fincar, Finpecia, Finax, Finast, Finara, Finalo, Prosteride, Gefina, Finasterid IVAX), dutasteride (Avodart, Avidart, Avolve, Duagen, Dutas, Dutagen, Duprost), Zoladex (goserelin acetate), Eulexin (flutamide), Lupron (leuprolide acetate)
    • Antihypertensives: prazosin (Minipress, Vasoflex, Hypovase)
    • Estrogens (Menest, Premarin, Premarin IV)
    • Acetylcholinesterase inhibitors (rivastigmine (Exelon), galantamine, (Reminyl, donepezil (Aricept), Tacrine.
    • Memantine (Namenda)
  14. Urinary obstruction in male PD patients as diagnosed by a urologist
  15. Active urinary tract infection.
  16. Patients with a history of chronic severe constipation (by self report)
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
23 participants (actual)

Study arms

  • Experimental
    solifenacin succinate (VESIcare)

    Drug: solifenacin succinate (VESIcare)

  • Placebo comparator
    placebo

    Drug: placebo

Interventions

  • Drugsolifenacin succinate (VESIcare)

    up to 10mg every day orally

  • Drugplacebo

    placebo matching solifenacin succinate (VESIcare) up to 10mg orally every day

06

What researchers measure

Primary outcomes

  1. Number of Micturations Per 24 Hour Period

    The primary objective of this study is to measure the efficacy of solifenacin succinate (VESIcare) in reducing the mean number of micturitions per 24 hour period in Parkinson's disease (PD) patients as measured by voiding diaries.

    Time frame: 12 weeks

Secondary outcomes

  1. Number of Urinary Incontinence Episodes Per 24 Hour Period

    This scale it the mean number of urinary incontinence episodes per 24 hour period, as assessed by a 3-day bladder diary. The goal is to examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity.

    Time frame: 12 weeks

  2. Unified Parkinson's Disease Rating Scale (UPDRS) Total

    To examine the effect of solifenacin succinate (VESIcare) on Parkinson's disease severity. The UPDRS total score ranges from 0 (no disability) to 199 (total disability).

    Time frame: 12 weeks

  3. Parkinson's Disease Quality of Life Scale (PDQOL)

    This scale is used to assess quality of life in Parkinson's Disease patients. Parkinson's disease quality of life scale has a possible point range from 37 (worst outcome) to 185 (best outcome). The goal of this outcome measure is to examine the effect of solifenacin succinate (VESIcare) on quality of life.

    Time frame: 12 weeks

  4. Number of Nocturia Episodes Per 24 Hour Period

    To examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity

    Time frame: 12 weeks

07

Results

Posted May 27, 2015

Participant flow

Participant flow — Overall Study
MilestoneSolifenacin Succinate (VESIcare)Placebo
Started1013
Completed912
Not completed11
Withdrew: Withdrawal by subject10
Withdrew: Lost to follow-up01

Outcome measures

PrimaryNumber of Micturations Per 24 Hour Period

The primary objective of this study is to measure the efficacy of solifenacin succinate (VESIcare) in reducing the mean number of micturitions per 24 hour period in Parkinson's disease (PD) patients as measured by voiding diaries.

Time frame:
12 weeks
Reported as:
Mean · Number of micturations per 24 hours
Number of Micturations Per 24 Hour Period
Number of micturations per 24 hoursSolifenacin Succinate (VESIcare)Placebo
Baseline8.78 ± 2.189.19 ± 3.46
Endpoint (12 weeks)8.00 ± 3.368.94 ± 3.06
Statistical analysis
  • Solifenacin Succinate (VESIcare) vs Placebo · ANCOVA · p = 0.53 · Effect size: 0.20This represents the effect size between solifenacin and placebo.
SecondaryNumber of Urinary Incontinence Episodes Per 24 Hour Period

This scale it the mean number of urinary incontinence episodes per 24 hour period, as assessed by a 3-day bladder diary. The goal is to examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity.

Time frame:
12 weeks
Reported as:
Mean · Number of incontinence episodes/24 hours
Number of Urinary Incontinence Episodes Per 24 Hour Period
Number of incontinence episodes/24 hoursSolifenacin Succinate (VESIcare)Placebo
Baseline1.48 ± 2.561.78 ± 1.27
Endpoint (12 weeks)0.30 ± 0.311.61 ± 1.40
Statistical analysis
  • Solifenacin Succinate (VESIcare) vs Placebo · ANCOVA · p = 0.01 · Effect size: 0.53
SecondaryUnified Parkinson's Disease Rating Scale (UPDRS) Total

To examine the effect of solifenacin succinate (VESIcare) on Parkinson's disease severity. The UPDRS total score ranges from 0 (no disability) to 199 (total disability).

Time frame:
12 weeks
Reported as:
Mean · units on a scale
Unified Parkinson's Disease Rating Scale (UPDRS) Total
units on a scaleSolifenacin Succinate (VESIcare)Placebo
Baseline25.00 ± 9.7025.67 ± 12.26
Endpoint (12 weeks)21.67 ± 9.5925.75 ± 8.76
Statistical analysis
  • Solifenacin Succinate (VESIcare) vs Placebo · ANCOVA · p = 0.22 · Effect size: 0.35
SecondaryParkinson's Disease Quality of Life Scale (PDQOL)

This scale is used to assess quality of life in Parkinson's Disease patients. Parkinson's disease quality of life scale has a possible point range from 37 (worst outcome) to 185 (best outcome). The goal of this outcome measure is to examine the effect of solifenacin succinate (VESIcare) on quality of life.

Time frame:
12 weeks
Reported as:
Mean · units on a scale
Parkinson's Disease Quality of Life Scale (PDQOL)
units on a scaleSolifenacin Succinate (VESIcare)Placebo
Baseline125.00 ± 20.95114.50 ± 10.73
Endpoint (12 weeks)116.00 ± 26.42112.92 ± 17.19
Statistical analysis
  • Solifenacin Succinate (VESIcare) vs Placebo · ANCOVA · p = 0.47 · Effect size: 0.27
SecondaryNumber of Nocturia Episodes Per 24 Hour Period

To examine the effect of solifenacin succinate (VESIcare) on urinary incontinence severity

Time frame:
12 weeks
Reported as:
Mean · Number of nocturia episodes per 24 hours
Number of Nocturia Episodes Per 24 Hour Period
Number of nocturia episodes per 24 hoursSolifenacin Succinate (VESIcare)Placebo
Baseline2.48 ± 1.591.92 ± 1.14
Endpoint (12 weeks)2.04 ± 1.961.78 ± 0.88
Statistical analysis
  • Solifenacin Succinate (VESIcare) vs Placebo · ANCOVA · p = 0.94 · Effect size: 0.11

Adverse events

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

Adverse event summary by group
GroupDeathsSeriousOther
Solifenacin Succinate (VESIcare)—0/10 (0%)4/10 (40%)
Placebo—0/13 (0%)0/13 (0%)
Most frequent other events
Most frequent other events
EventSolifenacin Succinate (VESIcare)Placebo
XerostomiaSkin and subcutaneous tissue disorders2/100/13
ConstipationGastrointestinal disorders1/100/13
urinary retentionRenal and urinary disorders1/100/13

Baseline characteristics

Age, Customized
Age, Customized(years)Solifenacin Succinate (VESIcare)PlaceboTotal
Age (years)67.6 ± 6.666.5 ± 9.366.96 ± 8.04
Sex: Female, Male
Sex: Female, Male(Participants)Solifenacin Succinate (VESIcare)PlaceboTotal
Female358
Male7815
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Solifenacin Succinate (VESIcare)PlaceboTotal
Hispanic or Latino112
Not Hispanic or Latino91221
Unknown or Not Reported000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Solifenacin Succinate (VESIcare)PlaceboTotal
American Indian or Alaska Native000
Asian000
Native Hawaiian or Other Pacific Islander011
Black or African American112
White81018
More than one race000
Unknown or Not Reported112
Unified Parkinson's Disease Rating Scale (UPDRS) ADL subsection (mean)
Unified Parkinson's Disease Rating Scale (UPDRS) ADL subsection (mean)(units on a scale)Solifenacin Succinate (VESIcare)PlaceboTotal
Mean9.50 ± 5.4011.23 ± 4.7610.48 ± 5.01
Unified Parkinson's Disease Rating Scale (UPDRS) Motor subsection (Part III)
Unified Parkinson's Disease Rating Scale (UPDRS) Motor subsection (Part III)(points)Solifenacin Succinate (VESIcare)PlaceboTotal
Mean12.60 ± 4.3814.69 ± 5.1913.78 ± 4.86
Unified Parkinson's Disease Rating Scale (UPDRS) Total score
Unified Parkinson's Disease Rating Scale (UPDRS) Total score(units on a scale)Solifenacin Succinate (VESIcare)PlaceboTotal
Mean24.00 ± 9.6725.08 ± 11.9324.61 ± 10.78
Parkinson's Disease Quality of Life (PDQOL) total score
Parkinson's Disease Quality of Life (PDQOL) total score(units on a scale)Solifenacin Succinate (VESIcare)PlaceboTotal
Mean124.10 ± 19.96115.31 ± 10.68119.13 ± 15.65

7 further baseline measures are reported on the registry.

08

Study locations

3 sites
  • University of Miami
    Miami, Florida 33136, United States
  • University of South Florida
    Tampa, Florida 33612, United States
  • Emory University
    Atlanta, Georgia 30329, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01018264
Lead sponsor
University of South Florida
Responsible party
Theresa Zesiewicz, MD (Professor of Neurology, University of South Florida) — Principal investigator
First posted
Nov 23, 2009
Start date
Jan 2010
Primary completion
Aug 2014
Completion
Aug 2014
Results posted
May 27, 2015
Last update
Nov 9, 2021

Study contacts

Theresa Zesiewicz, MD
principal investigator · University of South Florida

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

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.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

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

Start the discussion