JPRN-jRCT1041200023招募中未知
Exploratory examination about the gene background to affect the stool frequency change at the Linacrotide and Elobxibat hydrate administration. - Chronic Costipation 2020
akamura Masakatsu0 个研究点目标入组 50 人开始时间: 2020年6月26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
- 50
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
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •1)A disease name: Chronic constipation
- •2)Form: Functional constipation
- •3)Age: 20 years or older
- •4)Sex: Regardless of men and women
- •5) An index of the overall status: Performance Status (ECOG) is 0 or 1
- •6) Written patient compliance: After the informed consent that is enough on participating to this study, an agreement by the free will of the patients is obtained.
排除标准
- •1)The patients who take irritant cathartic day after day(However, the trial entry is possible if the patients doing one-off use internal use can establish the interval for stage Washout of 2W).
- •2)The patients with a history of the remedy in Lubiprostone, Linaclotide, Elobixbat hydrate.
- •3)The patients with the serious hepatic disorder ( AST(GOT) or ALT (GPT) 100IU/L or more).
- •4)The patients with serious renal disease.
- •5)The patients with the serious systemic disease with cancer, diabetes, heart disorder, and the like.
- •6)The patients with the pregnant or pregnant possibility.
- •7)The patients who participated in other clinical trials. (clinical study) within three months before study drug beginning of dosage.
- •8)The patients whom an anticholinergic drug, an antipsychotic drug, anti-Parkinson medicine, opioids are given, and chemical constipation is suspected in.
- •9)The patients who judged a study responsibility physician or a study allotment physician to be inadequate as study patients.
研究者
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