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Anterior quadratus lumborum block at lateral supra-arcuate ligament versus classical transmuscular quadratus lumborum block for postoperative analgesia in cesarean section

Anterior quadratus lumborum block at lateral supra-arcuate ligament versus classical transmuscular quadratus lumborum block for postoperative analgesia in cesarean section

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043063
Enrollment
Unknown
Registered
2021-02-04
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-05-24

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

Conditions

Regional block

Interventions

Group II:classical transmuscular quadratus lumborum block

Sponsors

Beijing Haidian Maternal & Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-II; 18-40 years old patients; 2. A normal singleton pregnancy with a gestation of at least 36weeks; 3. Patients scheduled for elective caesarean section performed under spinal anaesthesia; 4. Patients with BMI less than 30kg / m2; 5. Patients were aware of the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with puncture site infection; 2. Patients with blood coagulation disorders; 3. Patients allergic to local anesthetics; 4. Patients with serious cardiovascular disease and blood disease; 5. Patients with serious obstetrical complications; 6. The object of alcohol abuse; 7. Patients with previous thoracic or spinal surgery history; 8. Patients with cognitive dysfunction before operation and unable to cooperate with pain assessment; 9. Patients who failed to complete intraoperative data collection and postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
The activity and rest pain visual analogue scores(VAS) after surgery;the rescue analgesic after surgery;The blocked dermatomal coverage after block;

Secondary

MeasureTime frame
The first onset significant pain postoperatively;Post-24h vomit-nausea score;satisfaction survey;

Countries

China

Contacts

Public ContactYun Wang

Beijing Haidian Maternal & Child Health Hospital

wangyun129@ccmu.edu.cn+86 13521611825

Outcome results

None listed

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