The Effects of Popliteal Nerve Block on Pain and Nerve-Related Symptoms After Acute Achilles Tendon Rupture Repair Surgery: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Age 18 - 65

• ASA classification: I - III

• BMI \< 35 kg/m2

• Undergoing acute Achilles tendon rupture repair surgery as a day surgery procedure

Locations
Other Locations
Canada
Women's College Hospital
RECRUITING
Toronto
Contact Information
Primary
Didem Bozak
didem.bozak@wchospital.ca
416-323-6008
Time Frame
Start Date: 2026-01
Estimated Completion Date: 2028-03
Participants
Target number of participants: 80
Treatments
Experimental: Popliteal nerve (PN) block group
30 mL of 0.5% ropivacaine with 2.5 µg/ml of epinephrine
Sham_comparator: Placebo Nerve Block
1 mL of saline
Related Therapeutic Areas
Sponsors
Leads: Women's College Hospital

This content was sourced from clinicaltrials.gov