跳至主要内容
临床试验/KCT0008045
KCT0008045
已完成
未知

A 12 week, Randomized, Double-Blind, Placebo-Controlled, Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of BA on Inflammatory Bowel Disease(Ulcerative Colitis)

Hongcheon Institute of Medicinal Herb0 个研究点目标入组 30 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
未指定
发起方
Hongcheon Institute of Medicinal Herb
入组人数
30
状态
已完成
最后更新
3年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
2022年10月18日
最后更新
3年前
研究类型
Interventional Study
性别
All

研究者

发起方
Hongcheon Institute of Medicinal Herb

入排标准

入选标准

  • 1\) adults over 19 and under 70
  • 2\) Mayo Clinic Score (MCS) with a total score of 3 or more and 10 or less
  • 3\) A person who is able to maintain IBD treatment drugs (such as 5\-ASA) in accordance with IBD treatment standards and prescriptions by the person in charge of treatment
  • 4\) A person who agrees to participate in the human body application test and signs a written consent form prior to the commencement of the human body application test

排除标准

  • 1\) A person who is currently being treated for infectious diseases including severe cardiovascular system, immune system, respiratory system, hepatometer, kidney and urology system, nervous system, musculoskeletal system, mental health, and skin
  • 2\) A person with a history of forearm resection
  • 3\) Those who are likely to undergo bowel resection within 3 months
  • 4\) A person who has a history of solid cancer and blood cancer within five years;
  • 5\) People with autoimmune diseases including Crohn's disease
  • 6\) A person who has or has complications such as stenosis or perforation in the gastrointestinal tract
  • 7\) A person who has administered immunomodulators or biological agents such as systemic steroids, TNF\-a Inhibitors, Azathioprine, and MTX within 3 months of visit 1
  • 8\) Those who consume excess alcohol within one year (men \> 210 g/week, women \> 140 g/week) based on visit 1
  • 9\) BMI \= 30 kg/m2 factor
  • 10\) Patients with uncontrolled hypertension (measured after stabilizing for 10 minutes with systolic blood pressure of 160 mmHg or higher or diastolic blood pressure of 100 mmHg or higher)

结局指标

主要结局

未指定

相似试验