Evaluation of the Efficacy of Suprascapular Nerve Block in Adhesive Capsulitis
- Conditions
- Adhesive Capsulitis
- Registration Number
- NCT06176248
- Lead Sponsor
- CHU de Reims
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not yet recruiting
- Sex
- All
- Target Recruitment
- 62
Inclusion Criteria:<br><br> - Patient treated for adhesive capsulitis corresponding to a loss of passive amplitude<br> of more than 20° in external rotation elbow to body and/or abduction in relation to<br> the contralateral shoulder.<br><br> - Patient over 18 years of age<br><br> - Patient covered by a social security scheme<br><br> - Presence of an accompanying person on the day of the procedure for the return trip<br><br> - Patient having signed the consent form to participate in the study<br><br>Exclusion Criteria:<br><br> - Patient protected by law<br><br> - Pregnant women<br><br> - Patient who has had shoulder surgery less than six months old<br><br> - Patient unable to undergo rehabilitation within one month of surgery<br><br> - Allergy to one of the products used (anesthetic, iodinated contrast medium)<br><br> - Neuro-orthopedic disorder hampering clinical recovery<br><br> - Hemostasis disorder contraindicating block (no discontinuation of anticoagulants<br> according to SFAR recommendations, congenital hemostasis disorder)
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Constant score
- Secondary Outcome Measures
Name Time Method