Efficacy of adductor canal block (ACB) compared to ACB with infiltration of interspace between the popliteal artery and the capsule of the posterior knee (IPACK) after knee replacement surgery - a prospective randomised controlled trial

Phase 4

Recruiting

• Conditions: postoperative painpostoperative mobility; M17; Gonarthrosis [arthrosis of knee]

• Registration Number: DRKS00023090
• Lead Sponsor: Hospital of Traumatology and Orthopaedics

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-09-17
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

elective unilateral total knee arthroplasty due to osteoarthritis,
- BMI <38 kg/m2,
- ASA I-III,
- patient is motivated to follow the protocol of the trial.

Exclusion Criteria

- bilateral total knee arthroplasty,
- allergy or intolerance to the trial medication,
- long-term use of anticoagulants before surgery,
- steroid therapy in the last year,
- active malignancy,
- neurological or balance problems,
- the patient is already in another study.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain at rest using numeric pain rating scale at 7-8 AM of the first postoperative day

Secondary Outcome Measures

Name	Time	Method
Strength of quadriceps muscle using Oxford scale at 7-8 AM of of the first postoperative day