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临床试验/JPRN-jRCT1090220317
JPRN-jRCT1090220317Other4 期

The effect of postoperative scheduled intravenous acetaminophen in patients undergoing laparoscopic cholecystectomy-Standardization of postoperative pain management in a clinical pathway in Japan - - Scheduled intravenous acetaminophen(SIVA)

HIDEKI TANIGUCHI0 个研究点目标入组 100 人开始时间: 2017年12月22日最近更新:
适应症

试验速览

阶段
4 期
状态
Other
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • The inclusion criteria were patients aged 20 years or older who were classified as class I or II by the American Society of Anesthesiologists Physical Status (ASA-PS) scale.

排除标准

  • The exclusion criteria were as follows: patients with renal dysfunction (estimated creatinine clearance <20 mL/min or on-going haemodialysis), liver dysfunction(AST or ALT > 100 U/L) , and/or out of clinical pathway of LC in our hospital.

研究者

发起方
HIDEKI TANIGUCHI

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