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

University Hospital of North Norway

Status and phase: Completed; Phase 1

Conditions: Fecal Incontinence

Treatments: Procedure: 2. Biofeedback; Procedure: 1. Anal injection

Study type: Interventional

Funder types: Other

Identifiers

NCT00303030

Biofeedback or injections

Details and patient eligibility

About

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 [e-mail] tlf: [phone]

Enrollment: 126 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

• 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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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126 participants in 2 patient groups

1. Anal injection

Active Comparator group

Treatment:

Procedure: 1. Anal injection

2. Biofeedback

Active Comparator group

Treatment:

Procedure: 2. Biofeedback