NCT03397459

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
132

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2015

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
3 years until next milestone

First Submitted

Initial submission to the registry

December 21, 2017

Completed
22 days until next milestone

First Posted

Study publicly available on registry

January 12, 2018

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2018

Completed
Last Updated

January 12, 2018

Status Verified

December 1, 2017

Enrollment Period

4 years

First QC Date

December 21, 2017

Last Update Submit

January 11, 2018

Conditions

Cervicobrachial NeuralgiaLordosis

Keywords

cervicobrachial neuralgiasagittal balancelordosis

Outcome Measures

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)

    Day 1

Secondary Outcomes (1)

  • NDI

    Day 1

Interventions

Spine teleradiography EOSDIAGNOSTIC_TEST

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

HAMDAN

Besançon, 25000, France

RECRUITING

MeSH Terms

Conditions

Brachial Plexus NeuritisLordosis

Condition Hierarchy (Ancestors)

Brachial Plexus NeuropathiesPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNeuritisSpinal CurvaturesSpinal DiseasesBone DiseasesMusculoskeletal Diseases

Central Study Contacts

Noor HAMDAN

CONTACT

hmdnnoor@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 21, 2017

First Posted

January 12, 2018

Study Start

January 1, 2015

Primary Completion

December 31, 2018

Study Completion

December 31, 2018

Last Updated

January 12, 2018

Record last verified: 2017-12

Data Sharing

IPD Sharing
Will not share

Locations

FR(1)