临床试验/NCT01442961

NCT01442961已完成不适用

Postoperative Pain After Vaginal or Laparoscopic Hysterectomy: a Prospective Trial

Tampere University Hospital1 个研究点分布在 1 个国家目标入组 188 人开始时间: 2009年1月最近更新: 2013年4月10日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方: Tampere University Hospital
入组人数: 188
试验地点: 1
主要终点: Postoperative consumption of an opioid (oxycodone)

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The previous studies have shown that recovery after laparoscopic or vaginal hysterectomy is faster than after abdominal approach. The aim of this study is to evaluate postoperative pain after vaginal or laparoscopic hysterectomy. The primary outcome measurement is opioid consumption.

研究设计

研究类型: Interventional
分配方式: Non Randomized
干预模型: Parallel
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 69 Years（Adult, Older Adult）
性别: Female
接受健康志愿者: 否

入选标准

•Age 18 -69 years
•Gender . female
•ASA status 1-3
•Vaginal hysterectomy or laparoscopic hysterectomy

排除标准

•Body mass Index over 35
•Diabetes Mellitus
•Liver disease
•Allergies to pharmaceuticals used in the Study
•Present use of opioids
•Vaginal prolapse

结局指标

主要结局

Postoperative consumption of an opioid (oxycodone)

时间窗: 20 hours

the consumption of oxycodone will be monitored by recording the amount of the drug received via a commercially available patient controlled analgesia (PCA) pump

次要结局

NRS (numeral rating scale) of pain(20 hours)

研究者

发起方

Tampere University Hospital

申办方类型

Other

责任方

Principal Investigator

主要研究者

Arvi Yli-Hankala

professor

Tampere University Hospital

研究点 (1)

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