Clinical Trial

Popliteal Nerve Block for Acute Achilles Tendon Rupture Repair Surgery

Recruiting
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Summary
Achilles tendon rupture is common, yet the value of popliteal nerve block for postoperative pain control during surgical repair remains uncertain. Despite widespread use, evidence supporting its analgesic effectiveness is limited, and both popliteal nerve block and Achilles tendon repair carry risks of nerve injury. This randomized, placebo-controlled trial will evaluate whether adding a popliteal nerve block to standard systemic analgesia improves postoperative pain and reduces opioid use in patients undergoing acute Achilles tendon rupture repair. Secondary outcomes will examine the incidence and impact of nerve complications on recovery, including return to physical activity and functional performance.
Protocol Amendment History 1 change
notable Primary completion pushed: 2027-11 -> 2027-12 2026-04-24
Trial Details
NCT Number NCT06886815
Lead Sponsor Women's College Hospital
Conditions Acute Achilles Tendon Rupture
Enrollment 80 participants
Start Date 2026-03-17
Primary Completion 2027-12 (estimated)
Study Completion 2028-03 (estimated)
Updated on ClinicalTrials.gov 2026-04-23