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临床试验/EUCTR2009-015719-42-FR
EUCTR2009-015719-42-FR进行中(未招募)1 期

A 12-week, randomised, double-blind, placebo controlled trial to evaluate the efficacy, quality of life, safety and tolerability of prucalopride in male subjects with chronic constipation

Movetis NV0 个研究点目标入组 374 人开始时间: 2010年6月22日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Movetis NV
入组人数
374

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • 1. Subject is a male out-patient =18 years of age (no upper age limit).
  • 2. Subject has a history of constipation, i.e. reports an average of =2 spontaneous
  • bowel movements (SBM)/week and one or more of the following for at least 6
  • months before the selection visit:
  • a) Very hard (little balls) and/or hard stools for at least a quarter of the stools;
  • b) Sensation of incomplete evacuation following for at least a quarter of
  • c) Straining at defecation for at least a quarter of the time.
  • The above criteria are only applicable for SBMs, i.e. BMs not preceded within
  • a period of 24 hours by the intake of a laxative agent or by the use of an enema.
  • Subjects who never have SBMs are considered to be constipated and are
  • eligible for the trial.
  • 3. Subject agrees to stop his/her current laxative treatment and is willing to use
  • rescue medication according to the rescue rule [Dulcolax??(bisacodyl)/
  • Main inclusion criteria to be assessed at baseline (randomisation):
  • 1. During the run-in period, the subject reports an average of =2 SBM/week that
  • result in a feeling of complete evacuation (SCBM).*
  • This includes subjects who never have SBMs.
  • 2. Subject stopped his/her laxative treatment and did not use rescue mediation on
  • more than 75% of days during the run-in period.*
  • 3. Subject did not use disallowed medication during the run-in period.
  • * Excluding the first 7 days for subjects using medication influencing bowel habit.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Subjects in whom constipation is thought to be drug-induced.
  • 2. Subjects using any disallowed medication.
  • 3. Subjects suffering from secondary causes of chronic constipation.

研究者

发起方
Movetis NV

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