Adductor canal block combined with iPACK block and adductor canal block for postoperative analgesia and functional outcome after anterior cruciate ligament reconstruction: a randomized controlled trial

Phase 4

Recruiting

• Conditions: anterior cruciate ligament injury; adductor canal block; iPACK block; pain; functional outcome; anterior cruciate ligament reconstruction

• Registration Number: TCTR20200512007
• Lead Sponsor: none

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-05-12
• Study Completion: 2021-11-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

Consenting 54 patients, aged between 18 to 75 years old, ASA
physical status I-III, and scheduled to undergo elective anterior cruciate ligament reconstruction surgery

Exclusion Criteria

patient refusal
BMI > 35kg/m2
contraindication to neuraxial anesthesia and peripheral nerve block e.g. coagulopathy
known allergy to local anesthetic drugs or drugs used in the study
pre-existing neuromuscular disorders

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
postoperative pain score at rest and at movement at 6, 12, 18 and 24 hrs postoperative Numerical rating scale (NRS; 0-10)

Secondary Outcome Measures

Name	Time	Method
overall patient satisfaction at 24 hours postoperative Numerical rating scale (NRS; 0-10),hospital lenght of stay time to discharge out of hospital duration (hour),postoperative complications 24 hours postoperative events,postoperative morphine consumption and time to first analgesic requirement 24 hours postoperative amount and time ,postoperative fuctional outcome at 2 weeks, 6 weeks and 3 months postoperative Lysholm knee score and International Knee Documentation Committee (IKDC) score