Clinical Trial

Notch vs Midpoint Suprascapular Nerve PRF for Chronic Shoulder Pain

Study acronym: SUPRA-PRF
Recruiting
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Summary
This study aims to compare the effects of pulsed radiofrequency (PRF) treatment of the suprascapular nerve using suprascapular notch and midpoint approaches on pain, shoulder function, and muscle strength in patients with chronic shoulder pain due to rotator cuff tendinopathy. Patients will be randomly assigned to one of the two intervention groups. Clinical evaluations will include pain assessment using the Numeric Rating Scale (NRS), functional assessment using the Shoulder Pain and Disability Index (SPADI), and quality of life assessment using the Short Form-36 (SF-36). In addition, shoulder range of motion will be measured goniometrically, muscle thickness of the supraspinatus and infraspinatus will be evaluated by ultrasonography, and shoulder muscle strength will be assessed using an isokinetic dynamometer. Assessments will be performed at baseline, 24 hours, 1 month, and 3 months after the intervention. The results of this study are expected to provide evidence regarding the optimal approach for PRF treatment of the suprascapular nerve in patients with chronic shoulder pain.
Protocol Amendment History 1 change
critical Recruitment opened 2026-07-01
Trial Details
NCT Number NCT07502209
Lead Sponsor Ankara City Hospital Bilkent
Conditions Chronic Shoulder Pain, Rotator Cuff Tendinopathy
Enrollment 32 participants
Start Date 2026-05-07
Primary Completion 2027-06-30 (estimated)
Study Completion 2027-08-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-30