跳至主要内容
临床试验/NCT00348634
NCT00348634终止4 期

The Effects of Tegaserod on Orocecal Transit in Elderly Patients With Chronic Constipation

Novartis6 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年7月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
终止
发起方
Novartis
入组人数
60
试验地点
6
主要终点
Orocecal transit: Time of radioactive marker to reach the cecum using scintigraphy

研究概览

简要总结

This study will evaluate the effects of tegaserod on orocecal and colonic transit in patients over 65 years with chronic constipation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male & Females aged 65 and older
  • Patients must meet the criteria for chronic idiopathic constipation for at least 12 weeks
  • Patients must have had a colonoscopy within the past 5 years
  • Patients must pass a balloon expulsion test at screening
  • Patients must be able to comply and understand the use of a diary

排除标准

  • Patients with a clinically significant medical condition that would interfere with the patient completing the trial
  • Patients with loose stools at least once per week
  • Patients with IBS
  • Known allergies to the same class of drug and/or allergies to eggs
  • Patients who require the use of manual maneuvers to have a bowel movement
  • Other protocol-defined inclusion/exclusion criteria may apply.

结局指标

主要结局

Orocecal transit: Time of radioactive marker to reach the cecum using scintigraphy

次要结局

  • Whole gut transit and stomach emptying: Following 2 weeks of treatment, the rate of transit of food through the colon and stomach will be measured using scintigraphy

研究者

发起方
Novartis
申办方类型
Industry
责任方
Sponsor

研究点 (6)

Loading locations...

相似试验