跳至主要内容
临床试验/NCT01511627
NCT01511627撤回不适用

A Randomized Controlled Trial Comparing Postoperative Pain Following Total Abdominal Hysterectomy With General Anesthetic vs. Combined General and Spinal Anesthetic

University of Saskatchewan1 个研究点 分布在 1 个国家开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Total Morphine consumption

研究概览

简要总结

The investigators hypothesize that a spinal anesthetic administered prior to the induction of general anesthesia will result in reduced need for pain medication and reduced postoperative pain, as well as reduced hospital stay following a total abdominal hysterectomy.

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
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • American Society of Anesthesiologists' (ASA) I and II patients undergoing elective Total Abdominal Hysterectomy at the Saskatoon City Hospital
  • Lower transverse abdominal incision

排除标准

  • BMI > 40
  • The TAH is treatment for cancer
  • A history of regular opioid use
  • Any medical condition that would make a spinal inadvisable,
  • An allergy or medical condition that would make it inadvisable to receive the drugs used in this study (eg. Peptic ulcer disease), or
  • If you will also be having a salpingo-oophorectomy).

研究组 & 干预措施

General Anesthesia

Active Comparator

干预措施: General Anesthesia (control group) (Drug)

General Anesthesia + Spinal Anesthesia

Experimental

干预措施: General Anesthesia + Spinal anesthesia combined (Drug)

结局指标

主要结局

Total Morphine consumption

时间窗: Post-operative day 2

The primary outcome will be total opioid use per day, as recorded by the PCA pump and transcribed by the nursing staff in the PACU and on the post-operative ward.

Morphine consumption

时间窗: 1 day

The primary outcome will be total opioid use per day, as recorded by the PCA pump and transcribed by the nursing staff in the PACU and on the post-operative ward.

次要结局

  • Pain score on the VAS(On post-operative day 2 at 22:00)

研究者

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

Jacelyn Larson

Faculty

University of Saskatchewan

研究点 (1)

Loading locations...

相似试验

Randomized Controlled Trial Comparing Postoperative... | 临床试验