Vitala 12 Hour Wear Test With Convex Products
NCT01138709 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27
Last updated 2022-12-07
Summary
The primary objective of this phase II clinical trial is to assess the safety of the Vitala™ device during 12 hours of daily wear with convex products.
Conditions
- End Colostomy
Interventions
- DEVICE
-
Vitala
Vitala™ Continence Control Device
Sponsors & Collaborators
-
ConvaTec Inc.
lead INDUSTRY
Principal Investigators
-
Dheerendra Kommala, MD · ConvaTec Inc.
Study Design
- Allocation
- NA
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-02-28
- Primary Completion
- 2010-04-30
- Completion
- 2010-04-30
Countries
- United States
Study Locations
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