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Biofeedback for Dyssynergic Constipation

Biofeedback for Fecal Incontinence and Constipation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00127257
Enrollment
117
Registered
2005-08-05
Start date
1999-09-30
Completion date
2006-06-30
Last updated
2010-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Constipation

Keywords

Constipation, Biofeedback, Dyssynergia, Pelvic floor dyssynergia, Outlet dysfunction

Brief summary

Constipation affects 4% of adults in the United States (U.S.). An estimated half of constipated patients are unable to relax pelvic floor muscles during defecation, a type of constipation called pelvic floor dyssynergia (PFD). Biofeedback has been recommended for the treatment of constipation because uncontrolled studies over the past 10 years suggest that these treatments are as effective as medical or surgical management and involve no risk. However, placebo-controlled trials are still lacking. The aims of this study are: * to compare biofeedback to alternative therapies for which patients have a similar expectation of benefit; * to identify which patients are most likely to benefit; and * to assess the impact of treatment on quality of life.

Detailed description

This study is a long-term prospective, single-blind study comparing biofeedback for pelvic floor dyssynergia to a skeletal muscle relaxant drug (diazepam 5 mg two hours before attempted defecation) and to placebo medication. Prior to randomization, patients will first receive medical therapy (laxatives and education) for 4 weeks and only those remaining constipated will be randomized. Physiological tests of anal canal pressure during straining to defecate and ability to pass a 50-ml air filled balloon will be tested before and after treatment. Patients will keep a diary throughout baseline and treatment, and they will be reassessed at 3, 6, and 12 months follow-up. Treatment will consist of 6 clinic visits at 2-week intervals. The investigators will develop a detailed treatment manual for this disorder which would permit other investigators to replicate their study.

Interventions

BEHAVIORALPelvic floor retraining
BEHAVIORALBiofeedback
DRUGDiazepam

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Males or females ages 16 or above who have symptoms of constipation due to pelvic floor dyssynergia

Exclusion criteria

* Pregnancy (because of the possibility of randomization into the diazepam group) * Prior history of biofeedback treatment for pelvic floor disorders

Design outcomes

Primary

MeasureTime frame
Proportion of subjects reporting adequate relief per treatment group

Secondary

MeasureTime frame
Demonstrate association of improvement in quality of life with treatment outcome
Identify predictors of successful treatment outcome
Describe physiological mechanism of treatment effects

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026