NCT01207479View on ClinicalTrials.gov

Study to Assess the Safety and Performance of The VitalaTM Continence Control Device With Natura Moldable Skin Barriers

NACompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

September 30, 2010

Primary Completion Date

November 30, 2010

Study Completion Date

November 30, 2010

Conditions
Colostomy
Interventions
DEVICE

VitalaTM

A 43 day study design has been selected in order to capture meaningful safety and performance data of the Vitala™ device when used with these moldable products.

Sponsors

Lead Sponsor

ConvaTec Inc.
All Listed Sponsors
lead

ConvaTec Inc.

INDUSTRY

NCT01207479 - Study to Assess the Safety and Performance of The VitalaTM Continence Control Device With Natura Moldable Skin Barriers | Biotech Hunter | Biotech Hunter