CClinicalTrials.gg
Status unknownNCT03397459CNSBS-NCBESUpdated Jan 12, 2018

Cervicobrachial Neuralgia and Sagital Balance of the Cervical Spine

An observational study in Cervicobrachial Neuralgia and Lordosis, sponsored by Centre Hospitalier Universitaire de Besancon. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-01-12.

Sponsored by Centre Hospitalier Universitaire de Besancon · Observational

The sponsor has not verified this record recently (last verified Dec 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
132
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this observational study is to establish estimation of global lordosis of the cervical spine (from C3 to C7) in patients with cervicobrachial neuralgia.

Read the detailed description

The main judgement critearia is the estimation in degree of this lordosis measured on EOS radiographies, The study includes adults patients with non traumatic cervicobrachial neuralgia caused by discal hernia free from any previous spine surgery.

02

Conditions studied

  • Cervicobrachial Neuralgia
  • Lordosis

Keywords

  • cervicobrachial neuralgia
  • sagittal balance
  • lordosis
03

Who can participate

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

Study population

Patients suffering of cervicobrachial neuralgia in the hospital of BESANCON, FRANCE followed by a neurosurgeon.

Inclusion criteria

  • Adults (>18 years old)
  • Suffering of cervicobrachial neuralgia caused by cervical hernia on MRI diagnosed by a neurosurgeon
  • with social care rights

Exclusion criteria

Exclusion Criteria:

  • Post traumatic cervicobrachial neuralgia in the past 12 months
  • Anteriority of spine surgery
  • Pregnant patients
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
132 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testSpine teleradiography EOS
05

What researchers measure

Primary outcomes

  1. Low Cervical spine lordosis

    In degree, the angle between the lower plate of C2 and the lower plate of the last cervical vertebrea (physiologycally)

    Time frame: Day 1

Secondary outcomes

  1. NDI

    Pain questionnaires (score of 0 and 50)

    Time frame: Day 1

06

Study locations

1 of 1 sites recruiting
  • HAMDAN
    Besancon, 25000, France
    • Noor HAMDAN · Contact
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03397459
Lead sponsor
Centre Hospitalier Universitaire de Besancon
Responsible party
Sponsor
First posted
Jan 12, 2018
Start date
Jan 1, 2015
Primary completion
Dec 31, 2018 (estimated)
Completion
Dec 31, 2018 (estimated)
Last update
Jan 12, 2018

Study contacts

Noor HAMDAN
Contact
hmdnnoor@gmail.com

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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