跳至主要内容
临床试验/TCTR20200712001
TCTR20200712001招募中4 期

Ibuprofen and Intraperitoneal Lidocaine Instillation for Relieving Intraoperative Pain during Postpartum Mini-laparotomy Tubal Ligation: A Randomized Controlled Trial

Research Affairs, Faculty of Medicine, Khon Kaen university0 个研究点目标入组 92 人开始时间: 2020年7月12日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
92

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
Female

入选标准

  • 1. Postpartum women giving birth within 72 hours
  • 2. Completed family and desired for tubal sterilization
  • 3. American society of anesthesiology (ASA) physical status I
  • 4. Tubal ligation was not contraindicated.
  • 5. Written informed consent was given for tubal sterilization.
  • 6. Written informed consent was given for participating in the current study.

排除标准

  • 1. BMI 30 kg/m2 or higher
  • 2. Previous pelvic surgery
  • 3. Previous pelvic inflammatory disease
  • 4. Ibuprofen was contraindicated. Contraindication include
  • 4.1 Ibuprofen or NSAIDs allergy
  • 4.2 GFR < 30 ml/min
  • 4.3 Previous dyspepsia or gastritis, diagnosed by physician
  • 4.4 Current abdominal pain, dyspepsia, upper gastrointestinal tract bleeding
  • - Cardiovascular disease, including hypertension
  • - other contraindication
  • 5. Lidocaine allergy

研究者

发起方
Research Affairs&#44; Faculty of Medicine&#44; Khon Kaen university

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