A Randomized, Controlled, Clinical Trial of Biofeedback and Anal Injections as First Treatment of Fecal Incontinence
Primary Purpose
Fecal Incontinence
Status
Completed
Phase
Phase 1
Locations
Norway
Study Type
Interventional
Intervention
1. Anal injection
2. Biofeedback
Sponsored by
About this trial
This is an interventional treatment trial for Fecal Incontinence focused on measuring Fecal incontinence, Biofeedback, Patient Satisfaction, Quality of LifeTreatment Outcome, Injections
Eligibility Criteria
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
Sites / Locations
- Innlandssykehuset Hamar
- Anorektallaboratoriet, Østfoldsykehuset Sarpsborg
- Avdeling for gastroenterologisk kirurgi, University hospital of North Norway
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1. Anal injection
2. Biofeedback
Arm Description
Outcomes
Primary Outcome Measures
Incontinence measured by St.Marks incontinence score
Secondary Outcome Measures
Health related Quality of Life measures
Physiologic measures
Full Information
NCT ID
NCT00303030
First Posted
March 14, 2006
Last Updated
November 16, 2011
Sponsor
University Hospital of North Norway
Collaborators
Norwegian Foundation for Health and Rehabilitation
1. Study Identification
Unique Protocol Identification Number
NCT00303030
Brief Title
A Randomized, Controlled, Clinical Trial of Biofeedback and Anal Injections as First Treatment of Fecal Incontinence
Official Title
A Randomized, Controlled, Clinical Trial of Biofeedback and Anal Injections as First Treatment of Fecal Incontinence.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2011
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital of North Norway
Collaborators
Norwegian Foundation for Health and Rehabilitation
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence
Keywords
Fecal incontinence, Biofeedback, Patient Satisfaction, Quality of LifeTreatment Outcome, Injections
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
126 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1. Anal injection
Arm Type
Active Comparator
Arm Title
2. Biofeedback
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
1. Anal injection
Other Intervention Name(s)
Solesta
Intervention Description
Submucosal injection just above the linea dentata in the anal canal of 4 x 1 ml of dextranomere.
Intervention Type
Procedure
Intervention Name(s)
2. Biofeedback
Intervention Description
Training under the guidance of a physiotherapist with the help of a biofeedback device with an anal probe.
Primary Outcome Measure Information:
Title
Incontinence measured by St.Marks incontinence score
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Health related Quality of Life measures
Time Frame
2 years
Title
Physiologic measures
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barthold Vonen, M.D., Ph.D.
Organizational Affiliation
University of Tromsø, Norway
Official's Role
Study Director
Facility Information:
Facility Name
Innlandssykehuset Hamar
City
Hamar
Country
Norway
Facility Name
Anorektallaboratoriet, Østfoldsykehuset Sarpsborg
City
Sarpsborg
ZIP/Postal Code
1723
Country
Norway
Facility Name
Avdeling for gastroenterologisk kirurgi, University hospital of North Norway
City
Tromso
ZIP/Postal Code
9016
Country
Norway
12. IPD Sharing Statement
Learn more about this trial
A Randomized, Controlled, Clinical Trial of Biofeedback and Anal Injections as First Treatment of Fecal Incontinence
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