Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty

Phase 3

• Conditions: patients receiving bilateral total knee arthroplasty

• Registration Number: JPRN-UMIN000030996
• Lead Sponsor: Asahikawa Medical University Anesthesiology and Critical Care Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-01-25
• Study Completion: 2022-09-30
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

Not provided

Exclusion Criteria

history of complications Patients who can not evaluate NRS Patients with local anesthetics allergy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative 24h Numerical Rating Scale(NRS) at rest

Secondary Outcome Measures

Name	Time	Method
Postoperative NRS at rest (0,6,12,48h) Postoperative NRS during knee movement (0,6,12,24,48h) Postoperative Range of Motion (ROM)(12,24,48h) Postoperative effect of Sciatic nerve block (0,12,24h)