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NCT05360303 Clinical Trial

Electromyography in Thoracic Outlet Syndrome

Thoracic Outlet Syndrome Clinical Trial

— ENMG-AFC  

Official title:
Interest of Electroneuromyography in the Diagnosis of Thoracic Outlet Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05360303
Other study ID # RC22_0229
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 9, 2022
Est. completion date March 23, 2024

Study information
Verified date April 2024
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Record the ENMG data carried out systematically in patients treated by rehabilitation for thoracic outlet syndrome in order to assess their characteristics and judge the relevance of these data in the context of the diagnosis and their possible modifications following the rehabilitation treatment.

Recruitment information / eligibility
Status Completed
Enrollment 67
Est. completion date March 23, 2024
Est. primary completion date February 23, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Inpatient rehabilitation for thoracic outlet syndrome - Patients' agreement Exclusion Criteria: - < 18 years old - Not able to consent - Pregnancy - Musculoskeletal disorders of the upper limbs - Acute cardiac, pulmonary, metabolic or neurological diseases

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Department of Physical Medicine and Locomotive Rehabilitation (Nantes University Hospital) Nantes

Sponsors (1)
Lead Sponsor Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evaluation of the presence of ENMG abnormality and in particular on the medial cutaneous nerve of the forearm of patients with a clinical diagnosis of TOS Conduction abnormality of the medial cutaneous nerve of the forearm 0 Month
Secondary Evaluation of ENMG changes following rehabilitation treatment of patients evolution of electrophysiological changes following treatment 1 Month
Secondary Evaluation of ENMG changes following rehabilitation treatment of patients evolution of the Visual Analog Score for pain (scale from 0 to 10 ; 10 being the worst outcome) 1 Month
Secondary Evaluation of ENMG changes following rehabilitation treatment of patients evolution of the Quick Disabilities of the Arm, Shoulder and Hand Score (scale from 0 to 100 ; 100 being the worst outcome) 1 Month
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