drugset / Trial / NCT06524596

Study on Gynecological Laparoscopy Under Total Intravenous Anesthesia

NCT06524596

Completed 59 enrolled Wuhan Children's Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

To investigate the effect of preemptive analgesia with tartaric acid butorphanol on postoperative pain in gynecological laparoscopy under total intravenous anesthesia with remifentanil.This randomised, double-blind, placebo-controlled trial enrolled 60 patients undergoing elective gynaecological laparoscopy. The patients were divided into two groups: the butorphanol group (n = 30) and the control group (n = 29). Both groups received TIVA with propofol and remifentanil. Observing two groups of patients on the visual analog scale, the total consumption of rescue analogies, and the confidence of postoperative nausea and vomiting (PONV), and the patient satisfaction score.

Timeline

Start
2022-01-01
Primary completion
2022-12-31
Completion
2023-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Butorphanol Other / unclassified 0.02 mg/kg Intravenous
Background Propofol Small molecule 2 mg/kg
Background Remifentanil Small molecule 0.6 ug/kg

Indications

No indication recorded.