NL-OMON30232已完成不适用
The efficacy of intravenous versus rectal paracetamol: A randomized, prospective, double-blind placebo-controlled study - rectal versus intravenous paracetamol
适应症
试验速览
- 阶段
- 不适用
- 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
- 18 至 99（—）
入选标准
- •ASA class I-III
- •Patients undergoing lower abdominal laparotomies under general anesthesia
- •older tha 18 years
- •men and women
排除标准
- •Patients with a BMI >30.
- •Participation in a trial on investigational drugs within 3 months prior to the study.
- •Known hypersentivitity to paracetamol.
- •Known hypersentivitity to opioids.
- •Known history of hepatic, renal disease or other disease as judged by the investigators.
- •Those receiving chronic analgesic therapy.
- •Inability to perform VAS score.
- •Pregnancy or lactation.
- •Alcohol or drug abusus or history of alcohol/drug abusus.
- •Impaired liver function.
- •Any other reason which in the opinion of the investigator makes the patient unsuitable for participation in the study.
研究者
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