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Application of Liposomal Bupivacaine in Quadratus Lumborum Block for Analgesia and Rehabilitation After Hip Arthroplasty in Elderly Patients

Application of Liposomal Bupivacaine in Quadratus Lumborum Block for Analgesia and Rehabilitation After Hip Arthroplasty in Elderly Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120615
Enrollment
Unknown
Registered
2026-03-17
Start date
2025-09-09
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Postoperative Pain After Total Hip Arthroplasty (THA)

Interventions

Liposomal Bupivacaine Group:Administration of Liposomal Bupivacaine via Quadratus Lumborum Block
Non-Liposomal Bupivacaine Group:Administration of Levobupivacaine via Quadratus Lumborum Block

Sponsors

The Second Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Forty elderly patients undergoing elective hemiarthroplasty or total hip arthroplasty; 2. Age 60 to 80 years old, 3. ASA grade II or III.

Exclusion criteria

Exclusion criteria: 1.Patients with contraindications to regional anesthesia; 2.Patients allergic to any anesthetic agents; 3.Body weight <40 kg; 4.Patients with abnormal coagulation parameters or platelet counts; 5.Patients with preoperative cognitive impairment; 6.Patients with infection at the needle insertion site; 7.Patients declining to participate in the study;

Design outcomes

Primary

MeasureTime frame
Motor function recovery time;Pain scores at rest and during hip motion;

Secondary

MeasureTime frame
Cumulative consumption of opioids for patient-controlled intravenous analgesia.;

Countries

China

Contacts

Public ContactLu Jiahui

The Second Affiliated Hospital of Wenzhou Medical University

wzljh1207@163.com+86 18267852976

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026