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Effects of ultrasound-guided quadratus lumborum block at the lateral supra-arcuate ligament on postoperative pain and quality of recovery in patients undergoing open partial hepatectomy: a randomized controlled trial

Effects of ultrasound-guided quadratus lumborum block at the lateral supra-arcuate ligament on postoperative pain and quality of recovery in patients undergoing open partial hepatectomy: a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063291
Enrollment
Unknown
Registered
2022-09-03
Start date
2022-09-20
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

Liver tumor

Interventions

Group Q:operate quadratus lumborum block at the lateral supra-arcuate ligament
Group T:operate transversus abdominis plane block

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I - III; 2. Aged 18-65 years; 3. BMI 18.5-30.0 kg/m2; 4. Patients scheduled for elective partial hepatectomy.

Exclusion criteria

Exclusion criteria: 1. Severe liver and kidney dysfunction (Child-Pugh score grade C); 2. Severe respiratory and circulatory system disease (NYHA cardiac function level III or above); 3. Diabetes; 4. History of chronic pain; 5. Coagulation dysfunction, puncture site infection or trauma history; 6. Identify spinal deformities or expected ultrasonic anatomical abnormalities; 7. There are peripheral nerve diseases or sensory abnormalities in the innervated skin area; 8. Allergy to analgesics or local anesthetics; 9. Recent use of antipsychotic drugs, alcoholism or drug abuse; 10. History of abdominal surgery or trauma, and surgical scar may affect local anesthetic diffusion; 11. History of previous liver resection, tumor rupture or bleeding; 12. Refuse to participate.

Design outcomes

Primary

MeasureTime frame
Total morphine equivalent consumption;

Secondary

MeasureTime frame
Total morphine equivalent consumption ;Total morphine equivalent consumption;Total morphine equivalent consumption;Total morphine equivalent consumption;NRS score at 2h after operation;NRS score at 6h after operation;NRS score at 12h after operation;NRS score at 24h after operation;NRS score at 48h after operation;Time of first PCA after operation;Ramsay Sedation score ;Times of pressing analgesic pump ;Time of first rescue analgesia after operation;Postoperative remedial analgesic dosage;Recovery quality score (QoR-15) on the 1st and 2nd day after operation;Sleep quality score on the 1st and 2nd day after operation;Time of first getting out of bed after operation;First postoperative exhaust time;Length of postoperative hospitalization;Intraoperative remifentanil dosage;Intraoperative propofol dosage;Intraoperative mean arterial pressure;

Countries

China

Contacts

Public ContactYan Ming

Affiliated Hospital of Xuzhou Medical University

yiy3001@163.com+86 18052268329

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026