JPRN-jRCTs061220050招募中2 期
Improvement effect and safety of overactive bladder symptoms by 5-aminolevulinic acid (5-ALA) intake;Double-blind randomized placebo-controlled trial
Fukata Satoshi0 个研究点目标入组 100 人开始时间: 2022年8月29日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 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
- Interventional
入排标准
- 年龄范围
- >= 30age old 至 ot applicable（—）
- 性别
- All
入选标准
- •All of the following criteria must be met in order to
- •participate in this trial.
- •1.Patients with overactive bladder over 30 years
- •2.Patients with overactive bladder who consented
- •to participate in the study in writing
排除标准
- •If any of the following criteria are met, the patient
- •will not be allowed to participate in this trial.
- •1.Patients with organic disease of the urinary tract
- •2.Patients with neurogenic overactive bladder
- •3.Patients with malignant tumors of the urinary sys
- •4.Patients with cognitive dysfunction or psychiatri
- •c disorders that are difficult to conduct research
- •5.Patients who are allergic to 5-ALA
- •6.Patients with porphyria
- •7.Patients with drug hypersensitivity such as iron a
- •8.Pregnant women or patients who may become p
- •9.Patients who did not consent to participate in th
- •e study in writing
- •10.Patients disqualified by a doctor
研究者
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