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A clinical study on the analgesic effect of ultrasound-guided anterior lateral arcuate ligament superior quadratus lumborum block in patients with colon cancer radical resection

A clinical study on the analgesic effect of ultrasound-guided anterior lateral arcuate ligament superior quadratus lumborum block in patients with colon cancer radical resection

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063811
Enrollment
Unknown
Registered
2022-09-17
Start date
2022-09-17
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

Colon cancer in elderly patients

Interventions

Upper arch quadratus lumborum block group:Perform a supraarch quadratus lumborum block
Lateral approach quadratus lumborum block group:Lateral approach quadratus lumborum block

Sponsors

Hunan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. All patients are classified as ASA 2-3; 2. The patient's clinical data is complete and has good compliance.

Exclusion criteria

Exclusion criteria: 1. Those who have received pain relief treatment or have cognitive impairment before and after surgery and are unable to cooperate in pain assessment; 2. Patients with diabetes; 3. Patients with severe mental disorders; 4. Patients with severe heart, liver, and kidney dysfunction, alcohol abuse, and previous history of chest or spinal surgery; 5. Patients with coagulation disorders and blood system infections; 6. There is infection or tumor lesion at the puncture site; 7. Shock patients; 8. Failure to complete intraoperative data collection and postoperative follow-up; 9. Those who require surgical treatment at the puncture site; 10. Allergies to local anesthetics.

Design outcomes

Primary

MeasureTime frame
The anesthesia level was measured 5 minutes after the end of the block (T2);;According to the IOC-2 value (30 to 50), the intraoperative dose of opioids was recorded;Postoperative VAS scores at rest and during activity (postoperative resuscitation and extubation (T5), when leaving the pacu and returning to the ward (T6), 24 hours after surgery (T7), and 48 hours after surgery (T8));Supplementary analgesic drug dose 48h (T8) after operation;

Secondary

MeasureTime frame
Intraoperative IOC-1 and IOC-2 levels;vital signs;Adverse reaction score within 48h (T8) after operation;

Countries

China

Contacts

Public ContactZhang Yao

Changsha Central Hospital, Hunan Province/Hunan University of Traditional Chinese Medicine

1213845299@qq.com+86 18574540113

Outcome results

None listed

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