At a glance
ClinicalIndex Comparison RecordN/ACompleted· 124 enrolled
Drug / intervention
Minnesota Medical Technologies Anal Insert Devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Effects of the Minnesota Medical Technologies Anal Insert Device in Fecal Incontinence
In Brief
A clinical study evaluating Minnesota Medical Technologies Anal Insert Device for Fecal Incontinence. Completed, enrolled 124 participants across 1 site.
Detailed Summary
The purpose of this research is to test the effects of an inserted anal device on fecal incontinence (accidental bowel leakage) in patients who have persistent symptoms despite other conservative therapy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFecal Incontinence
CountriesUnited States
CollaboratorsMayo Clinic
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedApr 2019
Enrollment StartMay 2019
Primary CompletionFeb 2024
TodayJul 2026
First PostedApr 2, 2019
Enrollment StartMay 16, 2019
Primary CompletionFeb 20, 2024
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 7.3 years ago
Interventions
Minnesota Medical Technologies Anal Insert Devicedevice
Non-sterile soft, flexible, liquid-filled anal insert either 10 mm size or 13 mm size, meant for single use only