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Vitala 12 Hour Wear Test With Convex Products

2014-07-23 21:08:51 | BioPortfolio

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.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label

Conditions

End Colostomy

Intervention

Vitala

Location

Non-Institutional Investigator
Tucson,
Arizona
United States
85742

Status

Completed

Source

ConvaTec Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T21:08:51-0400

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Medical and Biotech [MESH] Definitions

The surgical construction of an opening between the colon and the surface of the body.

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In a clinical trial or interventional study, participants receive specific interventions according to the research plan or protocol created by the investigators. These interventions may be medical products, such as drugs or devices; procedures; or change...


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