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临床试验/NCT06252714
NCT06252714已完成不适用

Impact of Defecation Posture on Ease of Bowel Movements in Patients With a Rectocele.

TriHealth Inc.3 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
3
主要终点
Straining with bowel movements

研究概览

简要总结

The study aims to determine if defecation posture, when using a defecation posture modification device (DPMD), will improve ease of bowel movements in patients with pelvic organ prolapse, specifically rectoceles.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients with pelvic organ prolapse, including a rectocele (posterior compartment measurements to Stage 2 or greater) that endorse bowel dysfunction, based on our office standard screening questionnaires

排除标准

  • Anyone currently using a defecation posture modification device Unwillingness or unable to participate in the study Planned travel, inability to use device during the study period Patient preparing to undergo pelvic reconstructive surgery prior to the end of the study period Presence of ileostomy/colostomy Bowel disease such as Crohn's disease or Ulcerative Colitis Daily opiate use Wheelchair bound If device may pose fall or safety hazard risk to patient, such as need for walker or cane for ambulation.
  • Patients weighing over 250 lbs, per manufacturer guidelines for the device Inability to understand English Pregnant women

研究组 & 干预措施

Defecation Posture Modification Device

Experimental

Patients will be given a Squatty Potty Device

干预措施: Defecation Posture Modification Device (Device)

结局指标

主要结局

Straining with bowel movements

时间窗: 2 weeks

Patients will assess straining with bowel movement on a 0 -10 numeric scale. The scale is called straining or ease with bowel movements. The number 0 indicates no straining and the number 10 indicates maximal straining with bowel movement.

次要结局

  • Colorectal-Anal Distress Inventory 8(2 weeks)
  • Consistency of stool(2 weeks)
  • Use of laxative medication(2 weeks)
  • Ease of device use(2 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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