The analgesic efficacy between the iPACK block and genicular nerve blocks when combined with continuous adductor canal block for postoperative analgesia and functional outcome after Total knee arthroplasty: A randomized control trial

Phase 4

Completed

• Conditions: OA Knee going on total knee arthroplasty; Knee arthroplasty; Nerve block; Postoperative pain; Analgesia; analgesia

• Registration Number: TCTR20210727001
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-07-27
• Study Completion: 2022-04-04
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 132

Inclusion Criteria

Patient who was scheduled for total knee arthroplasty at King Chulalongkorn Memorial Hospital ASA class 1 to 3 ASA class 1 A normal healthy patient ASA class 2 A patient with mild systemic disease Mild diseases only without substantive functional limitations ASA class 3 A patient with severe systemic disease but not threaten to life Body mass index BMI between 18 to 40 kg/m2

Exclusion Criteria

1. refuse to participate this study, 2. unable to cooperate or cognitive impairment, 3. allergy to any drug in this study, 4. contraindication to neuraxial anesthesia, 5. contraindication to NSAIDs Ketorolac and Celebrex, 6. chronic opioids use or diagnosed of neuropathic pain, 7. unable to performed Time up and go test

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain score during movement 8 hours Visual Analog Scale