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Efficacy of ultrasound-guided adductor canal block with distal IPACK on analgesia and quality after total knee arthroplasty

Efficacy of ultrasound-guided adductor canal block with distal IPACK on analgesia and quality after total knee arthroplasty

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063214
Enrollment
Unknown
Registered
2022-09-01
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis of the knee

Interventions

Group A:ACB+IPACK
Group B:ACB+sham

Sponsors

Taizhou Hospital Affiliated to Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients undergoing elective total knee replacement; 3. American Society of Anesthesiologists (ASA) I-II; 4. No communication barriers, able to cooperate with intervention implementation and operation of patient-controlled analgesia equipment; 5. Participants should participate voluntarily and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with chronic pain; 2. Patients with contraindications of regional anesthesia (puncture site infection, trauma, etc.) or allergic to the anesthesia drugs to be used; 3. Coagulopathy (prothrombin time > 14.0s, partial thromboplastin time > 40s, platelet count 40U/L, creatinine level > 1.5 mg/dL); 5. Patients taking opioids for more than three weeks before surgery; 6. Body Mass Index (BMI) > 30 kg/m2.

Design outcomes

Primary

MeasureTime frame
Postoperative Visual Analogue Scale score;

Secondary

MeasureTime frame
Postoperative 24h hydromrophone consumption;Postoperative 48h hydromrophone consumption;Quality of Recovery-15 scale;Quadriceps muscle strength score;

Countries

China

Contacts

Public ContactZhu Congying

Taizhou Hospital Affiliated to Wenzhou Medical University

zcy0027@126.com+86 15958695321

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026