跳至主要内容
临床试验/JPRN-UMIN000028950
JPRN-UMIN000028950招募中未知

Exploratory study evaluating efficacy and safety of daikenchuto for the treatment of the postoperative abdominal pain or bloating in patients undergoing hepatectomy. - Exploratory study evaluating efficacy and safety of daikenchuto for the treatment of the postoperative abdominal pain or bloating in patients undergoing hepatectomy.

agasaki University0 个研究点目标入组 40 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
40

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Emergency surgery 2) With history of hepatectomy 3) Patient who have constitutional ICG excretory defect 4) With history of gastrointestinal surgery (excluding appendectomy) 5) Patient who are scheduled to enforce a gut surgery with hepatectomy (including biliary reconstruction) 6)With inflammatory bowel disease such as ulcerative colitis or Crohn disease (including anamnestic case) 7)With history of stoma 8)Patient who are scheduled for chemotherapy, radiation therapy or radiofrequency ablation therapy within 4 weeks before enrollment, during surgery or within 14 days after surgery (during individual study period) 9) Patient who took kampo medicine or lactobacillus preparation within 4 weeks before enrollment 10) Patient who are pregnancy, possibly pregnancy, considering pregnancy or lactating 11) Patient who are determined not applicable for the study by the physician

研究者

发起方
agasaki University

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