Skip to content

Analgesic effect of transversus abdominis plane block within multimodal analgesia after total abdominal hysterectomy: A double-blind randomized controlled trial

Analgesic effect of transversus abdominis plane block within multimodal analgesia after total abdominal hysterectomy: A double-blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040343
Enrollment
Unknown
Registered
2020-11-28
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

total abdominal hysterectomy

Interventions

TAP group:Ultrasound-guided Transversus Abdominis Plane Block 0.375% ropivacaine 40ml
Dexamethasone 5mg and Kepens 50mg before peeling
2. 6h after surgery, Kefen 60mg, 1-2d after surgery: PCA morphine, oral acetaminophen 650mgtid, Celebrex 200mgbid.
Control group:1. Dexamethasone 5mg and Kepens 50mg before peeling

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Female patients aged 18-65 years old with American Society of Anaesthesiologists (ASA) physical status I-II, scheduled for elective open gynecological surgery under general anaesthesia were assessed for eligibility.

Exclusion criteria

Exclusion criteria: (1) ASA physical status III or more; (2) pre-existing significant hepatic (liver enzymes more than two times normal values) or renal disease (estimated glomerular filtration rate <60 mL/min/1.73m2); (3) chronic diseases requiring regular corticosteroid or opioid treatment; (4) known allergy or contraindication to any of the drugs used in the study; (5) previous history of peptic ulcer, gastrointestinal bleeding or perforation; (6) inability to communicate due to psychiatric or nervous system diseases; (7) pregnant or breasting; (8) refuse to participate the study.

Design outcomes

Primary

MeasureTime frame
Pain;

Contacts

Public ContactZhiYu Geng

Department of Anesthesiology, Peking University First Hospital

gengzhiyu2013@163.com+86 010-83573218

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026