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Bilateral anterior quadratus lumborum block at lateral supra-arcuate ligament versus bilateral lateral quadratus lumborum block for analgesia in laparoscopic resection of colorectal cancer

Bilateral anterior quadratus lumborum block at lateral supra-arcuate ligament versus bilateral lateral quadratus lumborum block for analgesia in laparoscopic resection of colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053387
Enrollment
Unknown
Registered
2021-11-20
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-09-26

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

Conditions

regional block

Interventions

Experimental group1:Bilateral anterior quadratus lumborum block at lateral supra-arcuate ligament
Experimental group2:bilateral lateral quadratus lumborum block

Sponsors

Beijing Chaoyang Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-III level; aged 18 to 80 years; 2. Elective laparoscopic resection of colorectal cancer under general anesthesia; 3. BMI less than 30kg/m2; 4. Normal liver and kidney function; 5. The patients were aware of this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Puncture site infection; 2. Anticoagulation state; 3. Allergy to local anesthetics; 4. Serious cardiovascular disease, blood disease; 5. Alcohol abuse; 6. Combined with myasthenia gravis or Parkinson's disease or pregnancy; 7. History of previous abdominal or spinal surgery; 8. Cognitive dysfunction before surgery, unable to cooperate with pain assessment; 9. Intraoperative change to open surgery; 10. Failure to complete intraoperative data collection and postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
the total consumption of sufentanil in 24 hours;

Secondary

MeasureTime frame
Intra-op opioid consumption;Pain Numerical Scale at rest or on movementafter surgery;the rescue analgesic after surgery;satisfaction score;The occurrence of side effects such as nausea and vomiting within 24 hours after surgery;First postoperative patient controlled intravenousanalgesia compression time;time of first flatus,ambulation, oral intake and postoperative hospital stay;

Countries

China

Contacts

Public ContactWang Yun

Beijing Chaoyang Hospital Affiliated to Capital Medical University

wangyun129@ccmu.edu.cn+86 13521611825

Outcome results

None listed

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