At a glance
ClinicalIndex Comparison RecordN/ACompleted· 74 enrolled
Drug / intervention
SenSura Mio Convex Softdevice
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.
A Clinical Investigation Evaluating and Understanding Parameters Affecting the Performance of Ostomy Products
In Brief
A clinical study evaluating SenSura Mio Convex Soft for Ileostomy - Stoma and Colostomy. Completed, enrolled 74 participants across 9 sites in 4 countries.
Detailed Summary
The aim of the study is to obtain an understanding of relevant parameters affecting the performance of ostomy products.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIleostomy - Stoma, Colostomy
CountriesNetherlands, Norway, United Kingdom, United States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedAug 2015
Enrollment StartSep 2015
Primary CompletionMar 2016
TodayJul 2026
First PostedAug 7, 2015
Enrollment StartSep 1, 2015
Primary CompletionMar 1, 2016
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 10.9 years ago
Interventions
SenSura Mio Convex Softdevice
SenSura Mio Convex Soft is a CE marked ostomy product manufactured by Coloplast