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临床试验/JPRN-jRCT2080223112
JPRN-jRCT2080223112已完成3 期

Efficacy and safety trial of AJG555 in patients with chronic constipation (Phase 3 study)

EA Pharma Co., Ltd.0 个研究点目标入组 156 人开始时间: 2016年2月24日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
156

研究概览

简要总结

Treatment with AJG555 was initiated at 2 sachets once a day in patients with chronic constipation for both the 2-wk Confirmatory phase and 52-wk Extension phase. Based on their bowel condition, the dose was adjusted in accordance with the Dose Adjustment Criteria. As a result, the superiority of AJG555 versus the placebo was demonstrated. Moreover, the efficacy of AJG555 lasted for the entire 52-wk Extension phase. the tolerability of AJG555 in patients with chronic constipation was considered acceptable.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 15age old 至 ot applicable(—)
性别
All

入选标准

  • Patients with chronic constipation

排除标准

  • Patients with known or suspected organic constipation
  • Patients with known or suspected symptomatic constipation or drug-induced constipation

研究者

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