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临床试验/NCT06847022
NCT06847022已完成不适用

Efficacy of Ultrasound-guided Transversalis Fascia Plane Block (TFPB) in Controlling Postoperative Pain After Transverse Incision in Gynecologic Surgery

Thammasat University2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2024年11月4日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
2
主要终点
Postoperative 24 hours morphine requirement

研究概览

简要总结

Transversalis fascia plane block (TFPB) has been studied and has shown to be very effective in controlling postoperative pain after caesarean section but has not been studied in open gynecologic surgery with transverse incision. Inadequate pain control after open gynecologic surgery is associated with negative consequences such as chronic pelvic pain. The investigators aimed to evaluate the efficacy of TFPB in controlling postoperative pain after open gynecologic surgery with transverse incision.

详细描述

A randomized controlled trial study in which comparing US-guided TFPB vs conventional pain control in open gynecologic surgery

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who undergoing open gynecologic surgery under general anesthesia
  • Age 18 - 70 years
  • ASA Physical status I-III
  • Transverse incision

排除标准

  • Creatinine clearance is less than 30 ml/min
  • Body weight < 50 kg
  • Re-open surgery
  • Persistent chronic pelvic pain
  • Allergic to medications used in this study

研究组 & 干预措施

control

No Intervention

Patients in control group will receive general anesthesia for open gynecologic surgery.

TFPB

Experimental

Patients in this study group will receive general anesthesia and US-guided bilateral TFPB after wound closure.

干预措施: US-guided transversalis fascia plane block (Procedure)

结局指标

主要结局

Postoperative 24 hours morphine requirement

时间窗: 24 hours

次要结局

  • postoperative pain score(1 hour, 6 hours, 24 hours)
  • Side effects from postoperative opioids(24 hours)
  • Incidence of chronic pelvic pain(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

PREEYAPHAN ARUNAKUL

Assistant Professor

Thammasat University

研究点 (2)

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