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临床试验/NCT00303030
NCT00303030已完成1 期

A Randomized, Controlled, Clinical Trial of Biofeedback and Anal Injections as First Treatment of Fecal Incontinence.

University Hospital of North Norway5 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2006年5月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
126
试验地点
5
主要终点
Incontinence measured by St.Marks incontinence score

研究概览

简要总结

A short presentation of a randomized clinical trial of biofeedback and anal injections as a first treatment option of faecal incontinence.

Background: Faecal incontinence affects mainly women who have suffered sphincter disruption from vaginal delivery, but individuals of all ages can be affected. The treatment of this debility is not uniform between institutions or internationally. Often is surgical reconstruction of the anal sphincter performed, or other invasive, costly treatment options.

The study: We intend to conduct a randomized, controlled, clinical trial where we compare the effect of two less invasive, less costly treatment options as a first alternative: biofeedback and anal injections. Our hypothesis is that anal injections will give a better and more lasting effect than biofeedback. The primary endpoint will be change in faecal incontinence assessed by the St. Marks incontinence score. Secondary endpoints will include change in quality of life and several physiological parameters. We intend to include 62 patients in both groups, 124 all together, from 2 centres in Norway. The observation time is 2 years. We plan to include the first patient April 2006, and conclude the study by December 2010. This study can contribute to a more appropriate treatment-algorithm for these patients.

Study group:

  • Barthold Vonen MD PhD, Department of gastroenterological surgery, University Hospital of North Norway
  • Rolv-Ole Lindsetmo MD PhD, Department of gastroenterological surgery, University Hospital of North Norway
  • Arvid Stordahl MD PhD., Department of Surgery, Østfold Hospital Fredrikstad
  • Ylva Sahlin MD PhD, Department of Surgery, Innlandet Hospital Hamar
  • Trond Dehli, MD, Department of gastroenterological surgery, University Hospital of North Norway
  • Kjersti Mevik, Stud. Med, University of Tromso

Project manager: Trond Dehli

Funding, approvals, publication: This study is funded from Northern Norway Regional Health Authority and The Institution of Norwegian Health- and rehabilitation-organizations. It has been approved by the Regional Committee for Medical Research Ethics and Norwegian Social Science Data Services. The results will be published in an international peer-reviewed journal after the Vancouver-convention's guidelines. The results will also be presented at national and international conferences.

Contact:

Trond Dehli, Department of gastroenterological surgery, University hospital North Norway, Breivika, 9038 Tromsø trond.dehli@unn.no tlf: +47 776 26 000

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
Single (Outcomes Assessor)

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

  • Fecal incontinence lasting more than 6 months
  • St. Marks score of 4 or more
  • No known local or general neurological disease
  • 18 years or older
  • No constipation

排除标准

  • Total rupture of the sphincter of more than 120 degrees
  • Diabetes mellitus with late complications (neurological og cardiovascular)
  • Ulcus simplex/rectal ulcus
  • Anal/rectal prolapse
  • ileo-anal anastomosis
  • Cancer recti or cancer ani last 2 years
  • Pregnancy

结局指标

主要结局

Incontinence measured by St.Marks incontinence score

时间窗: 2 years

次要结局

  • Health related Quality of Life measures(2 years)
  • Physiologic measures(2 years)

研究者

发起方
University Hospital of North Norway
申办方类型
Other
责任方
Sponsor

研究点 (5)

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