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Sacral ESP Block for Postoperative Analgesia in Pilonidal Sinus Surgery
NCT07534488Recruiting
- Sponsor
- Istanbul Medipol University
- Start
- Apr 2026
- Primary completion
- Aug 2026
- Countries
- 1
01
Overview
Randomised, open-label trial (2 arms), sponsored by Istanbul Medipol University. Primary endpoint: Total postoperative rescue analgesic (opioid) consumption at 24 hours. Started Apr 2026; status: recruiting.
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