跳至主要内容
临床试验/NCT00985569
NCT00985569撤回不适用

Surveying The Outcomes Of Lubiprostone (The STOOL Study): The Effect of Lubiprostone on Reducing the Number of Medications Prescribed to Nursing Home Residents and Its Impact on Selected Quality Indicators

Synergy Health Solutions3 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2009年11月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
105
试验地点
3
主要终点
To determine the overall reduction in the number of oral medicines taken by each NH resident at enrollment and at 60 days.

研究概览

简要总结

The purpose is to assess the efficacy, clinical outcomes, and potential Quality Indicator benefits associated with the use of Lubiprostone in nursing home residents with a confirmed diagnosis of chronic idiopathic constipation.

详细描述

The study is a prospective, observational, open-label, non-placebo, controlled study to measure the effects of Lubiprostone on CIC in nursing home residents. All clinical sites will follow a common protocol using standardizes definitions in which eligible patients will be asked to participate in the proposed study. During the course of the study, various selected parameters will be measured and compared to establish the clinical efficacy of Lubiprostone in the treatment of CIC.

The study sample (N=105) will be comprised of nursing home residents with a confirmed diagnosis of CIC. A power analysis generated a sample size of 97 residents. To protect the validity of the test, 8 residents were added to the final study sample to allow for losses to followup. Therefore, a final sample size of 105 residents was identified for the study.

Patients meeting the inclusion criteria will be recruited for participation in the study. 3 sites in Central Florida with multiple Nursing Homes per site will be recruited to participate in the proposed study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patients must meet all of the following criteria to be eligible for the study:
  • Adult men and women nursing home residents;
  • Confirmed diagnosis of CIC using Rome criteria;
  • Prescribed two or more laxatives, at recruitment;
  • Taking 9 or more oral medicines (including prescription, OTC and prn)
  • Free from conditions likely to be fatal within six months;
  • Able to read or understand English; and
  • Able and willing to provide informed consent or has a guardian/agent who can provide consent.

排除标准

  • Currently pregnant;
  • Presence of megacolon;
  • Presence of rectal sigmoid cancer;
  • Presence of colon cancer;
  • Presence of anal incompetence;
  • Conditions likely to be fatal within six months;
  • Taking 8 or fewer medicines;
  • Enrolled in hospice;
  • Non-English speaking patients; and
  • Unwilling or unable to provide informed consent and has no guardian/agent.
  • Expected to be discharged within 3 months.

结局指标

主要结局

To determine the overall reduction in the number of oral medicines taken by each NH resident at enrollment and at 60 days.

时间窗: 60 days

次要结局

  • Reduce the number of oral medicines being taken by any nursing home resident from 9 or more to fewer than 9. (Quality Indicator Number 6)(60 days)
  • To compare the occurrence of fecal impaction during a 60-day period prior to initiating Lubiprostone with a 60 day period after initiating Lubiprostone. (Quality Indicator Number 11)(60 days)
  • To compare the occurrence of fecal incontinence during a 60-day period prior to initiating Lubiprostone with a 60 day period after initiating Lubiprostone.(60 days)

研究者

发起方
Synergy Health Solutions
申办方类型
Other

研究点 (3)

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