Skip to content

Influence of ultrasound- guided quadratus lumborum block with dexamethasone and ropivacaine on postoperative pain in patients undergoing lower uterine cesarean section

Influence of ultrasound- guided quadratus lumborum block with dexamethasone and ropivacaine on postoperative pain in patients undergoing lower uterine cesarean section

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089825
Enrollment
Unknown
Registered
2024-09-18
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Pain after caesarean section of lower uterus

Interventions

control group:20ml of 0.35% ropivacaine was used for each side
observation group:The drug formula of each side was 0.35% ropivacaine + dexamethasone 0.1mg/kg, 20ml in total

Sponsors

Peking University Third Hospital Yanqing Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
23 Years to 35 Years

Inclusion criteria

Inclusion criteria: (1) full-term pregnancy, singleton, primipara/multipara; (2) Age 23-35 years old, height 155-170cm, weight 50-90kg; (3) ASA grade I and II.

Exclusion criteria

Exclusion criteria: (1) There were contraindications to spinal anesthesia; (2) patients allergic to local anesthetics or opioids; (3) patients with sinus bradycardia and III degree atrioventricular block; (4) patients with history of chronic pain; (5) patients with communication disorders.

Design outcomes

Primary

MeasureTime frame
Weight, height, gestational age and age;Visual analogue scale (VAS) visual pain score;The dosage of sufentanil and the pressing times of analgesic pump within 48 h after operation were recorded;

Secondary

MeasureTime frame
Incidence of complications;

Countries

China

Contacts

Public ContactWu Xiaowen

Peking University Third Hospital Yanqing Hospital

wuxiaowenxdf@163.com+86 186 1180 7205

Outcome results

None listed

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