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NCT00515853 Clinical Trial

The Role of Biofeedback in Improving Continence After Anterior Resection

Fecal Incontinence Clinical Trial

Official title:
The Role of Biofeedback in Improving Continence After Anterior Resection

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00515853
Other study ID # RHM GSU 0132
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 27, 2006
Est. completion date May 13, 2010

Study information
Verified date January 2022
Source University of Southampton
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether biofeedback exercises improve anal continence after anterior resection for rectal cancer.

Description:

See above

Recruitment information / eligibility
Status Completed
Enrollment 121
Est. completion date May 13, 2010
Est. primary completion date May 13, 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Rectosigmoid or rectal cancer Exclusion Criteria: - Inoperable

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Biofeedback
Biofeedback sessions or biofeedback exercises

Locations
Country Name City State
United Kingdom Southampton General Hospital Southampton Hampshire

Sponsors (1)
Lead Sponsor Collaborator
University of Southampton

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cleveland Clinic Incontinence (CCI) Score The Cleveland Clinic incontinence score (CCI) is an anal incontinence severity score. It is easy to use and gives the patient a score of 0 to 20, where zero equates to perfect continence and twenty equates to complete anal incontinence. 1 year
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