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Ultrasound-guided quadratus lumbar block versus transverse abdominal fascial block for perioperative analgesia in patients undergoing laparoscopic colorectal cancer surgery: a randomized, controlled trial

Ultrasound-guided quadratus lumbar block versus transverse abdominal fascial block for perioperative analgesia in patients undergoing laparoscopic colorectal cancer surgery: a randomized, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066065
Enrollment
Unknown
Registered
2022-11-23
Start date
2022-11-14
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Analgesic effect of nerve block anesthesia

Interventions

QL group:quadratus lumbar block
TAP group: transverse abdominal fascial block

Sponsors

QILU HOSPITAL OF SHANDONG UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who underwent laparoscopic colorectal cancer surgery in our hospital 2. Age 18-80 years old, gender is not limited 3. ASA Grade I~II 4. Those who have a clear understanding, voluntarily participate in the study, and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1.Peripheral nerve block contraindications 2. Those who are allergic to local anesthetic drugs 3. Drug abusers (opioids, cortisols) 4. BMI> 35kg/m2 and BMI<18kg/m2 5. Any known heart failure, liver failure, chronic kidney disease 6. Endocrine diseases 7. Those who have undergone secondary open surgery 8. Patients with abnormal coagulation function and severe anemia.

Design outcomes

Primary

MeasureTime frame
Remifentanil dosage;

Secondary

MeasureTime frame
Changes in vital signs (heart rate, systolic/diastolic pressure, mean arterial pressure, BIS, and pain index) at various time points during surgery (baseline entry, establishment of pneumoperitoneum, 15 minutes after pneumotheta, 30 minutes after pneumotheta, 45 minutes after pneumoperitoneum, 60 minutes after pneumoperitoneum, op;Pain scores of 0h, 6h, 12h, 24h after the end of surgery;Postoperative recovery (nausea and vomiting, time to get out of bed, time to gas, length of hospital stay, adverse events, etc.).;White blood cell count, neutrophil count and its proportion, urea nitrogen value, creatinine value;

Countries

china

Contacts

Public ContactSun Baozhu

QILU HOSPITAL OF SHANDONG UNIVERSITY

baozhuql@126.com18560083765

Outcome results

None listed

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