N/A
N=20
The Use of an "Anal-Tape" in Patients With Fecal Incontinence
Fecal Incontinence
Bottom Line
View on ClinicalTrials.gov: NCT02989545 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcome: Primary: Any Improvment in the Fecal Incontince Quality of Life Scale (FIQoLs) — 2.8; 3.3; 1.9; 2.5 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Anal Tape (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Shaare Zedek Medical Center
- Primary completion
- Dec 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Any Improvment in the Fecal Incontince Quality of Life Scale (FIQoLs) |
2.8; 3.3; 1.9; 2.5; 3.1; 3.5 | — |
| SECONDARY A 50% Reduction in the Number of Episodes of FI Per Week |
0; 5 | — |
| SECONDARY Mean Wexner Score |
11.9; 10.3 | — |
| SECONDARY Mean Redction in Wexner Scale Compared to Baseline |
0.6; 1.95 | — |
| SECONDARY General Satisfaction |
80 | — |
| SECONDARY Willingness of the Patient to Continue Using the Anal Tape After the Study. |
90 | — |
Summary
Fecal incontinence (FI), defined as the involuntary passage of stool for more than 3 months and is a devastating disease. The negative impact on quality of life has been consistently demonstrated. The prevalence of FI is probably underestimated in most studies. Currently conservative treatment is only modestly effective and surgical treatment is complex and expensive with less than optimal efficacy.
The investigators developed an "anal tape" using a commercially available elastic band with a special adhesive that is approved for use in the skin. A special design of the tape can be applied to the skin surrounding the anus providing support and additional pressure forces to the anal sphincter.
This is a 4 week, prospective, non blinded, cross-over study to explore the efficacy and safety of this device in patients with FI. The primary endpoint will be improvement in quality of life.
Eligibility Criteria
Inclusion Criteria
- >18 years old
- Fecal incontinence for more than 6 months
- Willing to participate
- Understand the study procedures
- Is able to apply and remove the "anal tape" without significant assistance of others.
- Have done sigmoidsocopy or colonoscopy and anal manometry within five year of screening visit
Exclusion Criteria
- Advanced full thickness rectal prolapse.
- Injured, inflamed or any significant disease in the peri-anal skin.
- Allergy to any component of the device, either known or developed during testing in the screening visit.
- Moderate to severe proctitis of any etiology.
Data sourced from ClinicalTrials.gov (NCT02989545). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.