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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03397459
Other study ID # P/2016/284
Secondary ID
Status Recruiting
Phase N/A
First received December 21, 2017
Last updated January 11, 2018
Start date January 1, 2015
Est. completion date December 31, 2018

Study information

Verified date December 2017
Source Centre Hospitalier Universitaire de Besancon
Contact Noor HAMDAN
Email hmdnnoor@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 132
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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:

- Post traumatic cervicobrachial neuralgia in the past 12 months

- Anteriority of spine surgery

- Pregnant patients

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Spine teleradiography EOS


Locations

Country Name City State
France HAMDAN Besancon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Low Cervical spine lordosis In degree, the angle between the lower plate of C2 and the lower plate of the last cervical vertebrea (physiologycally) Day 1
Secondary NDI Pain questionnaires (score of 0 and 50) Day 1
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