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临床试验/IRCT2013072810765N4
IRCT2013072810765N4已完成2 期

Clinical trial of analgesic effect of intraperitoneal Bupivacaine-Petidine infiltration compared with intravenous after diagnostic gynecologic laparpscopy

Tabriz University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
90

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
20 years 至 38 years(—)
性别
Female

入选标准

  • Women with 20-38 years old; candidated for gynecologic diagnostic Laparoscopy; patients with ASA physical status I and II; patients who will give written informed consent
  • Exclusion criteria: Women with ASA physical status III or higher;patients who received analgesic; patients who had contraindication for NSAIDs or Paracetamol like peptic ulcer; coagulopathy; renal failure;hepatic failure; allergy

排除标准

  • 未提供

研究者

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