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Effect of transverse abdominis plane block combined with quadratus lumbar block on postoperative analgesia after cesarean section

Effect of transverse abdominis plane block combined with quadratus lumbar block on postoperative analgesia after cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112672
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-11-28
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

After cesarean section

Interventions

Observation group:After cesarean section, bilateral quadratus lumborum block and transverse abdominis plane block were performed, and the patients were connected to the patients intravenous self-contr
Control group:After bilateral transverse abdominis plane block after cesarean section, an intravenous self-controlled analgesia (PCIA) pump set to a standard background dose will be connected

Sponsors

Leshan City Central District Maternal and Children Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Age 18-45 years old; 2. ASA classification I-II; 3. Elective cesarean section under combined spinal-epidural anesthesia; 4. Single pregnancy >=37 weeks; 5. Voluntarily participate and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. BMI > 40 kg/m^2 (based on puncture safety and feasibility of ultrasound imaging); 2. Known allergies to study drugs such as ropivacaine, sufentanil, or nalbuphine; 3. Skin infection at the puncture site; 4. Presence of cognitive impairment, history of psychiatric disorders, or inability to understand pain scoring tools; 5. Long-term use of opioids or a history of chronic pain; 6. Complicated by severe central/peripheral nervous system diseases, cardiovascular diseases, or liver and kidney dysfunction; 7. Severe pregnancy complications (such as preeclampsia, HELLP syndrome).

Design outcomes

Primary

MeasureTime frame
Postoperative incision pain score;Postoperative contraction pain score;Postoperative rescue analgesia rate;

Secondary

MeasureTime frame
Time to first salvage analgesia after surgery;The number of effective compressions of the analgesic pump after surgery;Postoperative recovery indicators;Incidence of adverse reactions;Postoperative analgesic satisfaction;

Countries

China

Contacts

Public ContactLinjing Li

Leshan City Central District Maternal and Children Health Hospital

897718643@qq.com+86 187 8458 9810

Outcome results

None listed

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