Skip to content

A randomized controlled study on the effect of lumbar quadratus block on analgesia after cesarean section

A randomized controlled study on the effect of lumbar quadratus block on analgesia after cesarean section

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035973
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-08-22
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Cesarean section

Interventions

The first group:Quadratus lumborum block combined with patient-controlled intravenous analgesia
The second group:Epidural morphine combined with patient-controlled intravenous analgesia
The third group:Simple patient-controlled intravenous analgesia

Sponsors

Department of Anesthesiology, Guangdong Second Provincial General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. 90 patients (ASA I-II, aged 18-40 years) with singleton pregnancy and gestation time more than 37 weeks, body mass index ((BMI) 20-40kg/ m ^ 2) were selected for elective lower uterine segment transverse incision cesarean section under combined spinal-epidural anesthesia. 2. They were able to perform postoperative resting, exercise and visceral pain VAS scores, and were familiar with the use of patient-controlled intravenous analgesia pump. 3. Sign the informed consent for postoperative analgesia and agree to the use of nerve block for postoperative analgesia.

Exclusion criteria

Exclusion criteria: 1. Contraindications to spinal or regional anesthesia; 2. History of allergy to drugs used in this study; 3. Body mass index less than 20kg/ m ^ 2 or greater than 40kg/ m^2; 4. Preeclampsia; 5. History of chronic pain or long-term use of opioids; 6. Patients who are unable to understand or use the verbal pain score system or patient-controlled analgesia (PCA) pump. 7. The failure or poor effect of spinal anesthesia during operation was changed to general anesthesia, and the patients who could not cooperate with postoperative visit or dropped out of this study.

Design outcomes

Primary

MeasureTime frame
Postoperative dosage of sufentanil;

Secondary

MeasureTime frame
Number of PCA;VAS score (rest, exercise, visceral pain);Exhaust time;Sedation and comfort score;Hospitalization time;Height of fundus of uterus;Serum PRL concentration;Additional demand for analgesia;

Countries

China

Contacts

Public ContactZhang Hui

Guangdong Second Provincial General Hospital

Mazui_fanqisen@163.com+86 13719136792

Outcome results

None listed

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