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Ultrasound-guided adductor nerve block combined with lateral femoral cutaneous nerve block on postoperative pain management in total knee arthroplasty: A randomized controlled trial

Ultrasound-guided adductor nerve block combined with lateral femoral cutaneous nerve block on postoperative pain management in total knee arthroplasty: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015832
Enrollment
Unknown
Registered
2018-04-23
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

osteoarthritis

Interventions

Group A:adductor nerve block+lateral femoral cutaneous nerve block+Posterior capsule injection
Group B:adductor nerve block+lateral femoral cutaneous nerve block
Group C:adductor nerve block+Posterior capsule injection
Group D:adductor nerve block
Group E:blank control

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients ready for unilateral primary total knee arthroplasty for osteoarthritis with the age of 55 to 80 years old, BMI of 2035 kg/m2, and the risk grade of American Society of Anesthesiologists before operation I-III.

Exclusion criteria

Exclusion criteria: Those patients with a history of septic arthritis,rheumatic disease, excessive drinking and opioid consumption,patients who are allergic to medications used, with nerve affection of the legs and inability to understand the numeric rating scales (NRS), patients who have severe osteoarthritis with knee deformity, mental disorder, and ulcer in digest track were excluded.

Design outcomes

Primary

MeasureTime frame
Pain;knee range of motion;opioid consumption;postoperative hospital stays;WOMAC score;

Countries

China

Contacts

Public ContactPengde Kang

West China Hospital, Sichuan University

kangpd@163.com+86 18980601953

Outcome results

None listed

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