Clinical Trial

Preoperative Versus Postoperative Interscalene Block in Arthroscopic Rotator Cuff Repair

Study acronym: ISB-ARCR
Not Yet Recruiting
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Summary
This study is evaluating whether the timing of an interscalene nerve block affects pain control and recovery after arthroscopic rotator cuff repair surgery. An interscalene block is commonly used to reduce pain after shoulder surgery. However, it is not known whether administering the block before surgery or after surgery provides better outcomes. Participants undergoing arthroscopic rotator cuff repair are assigned to receive the interscalene block either before the surgical incision or after completion of the procedure. The study compares postoperative pain levels, opioid medication use, length of hospital stay, and ultrasound imaging quality during block administration between the two groups. Functional recovery is also assessed using patient-reported outcome measures during follow-up. The investigators hypothesize that administration of the interscalene block before surgery may provide superior early pain control and reduce postoperative opioid requirements while maintaining similar functional outcomes compared with administration after surgery.
Trial Details
NCT Number NCT07689448
Lead Sponsor Istinye University
Conditions Rotator Cuff Tear Repair, Interscalene Blocks, Rotator Cuff Tears
Enrollment 42 participants
Start Date 2026-07-13
Primary Completion 2026-10-01 (estimated)
Study Completion 2026-10-20 (estimated)
Updated on ClinicalTrials.gov 2026-07-08