78
Participants
Start Date
April 30, 2009
Primary Completion Date
January 31, 2010
Study Completion Date
January 31, 2010
Usual
All subjects will wear their usual pouching system for the first 21 days of the study.
Natura®
All subjects will wear the Natura® Flexible Skin Barrier with Flange (Stomahesive® or Durahesive®) in the US and Natura® Stomahesive® Flexible Skin Barrier with Flange in Europe for 14 days.
Vitala™
"After the successful completion of Stages 1 and 2, subjects will enter the ramp up schedule to allow the subject to adjust to the device. This consists of weekly increases in wear time of the Vitala™ device beginning with 4 hours of daily wear per week (Days 36 to 42), followed by 6 hours of daily wear time per week (Day 43 to 49), followed by 8 hours of daily wear time (Days 50 to 56) and progressing to 12 hours of daily wear per week (Day 57 to 215)."
Mt. Sinai Hospital, New York
Washington County Hospital, Hagerstown
Private Practice, Triwalk
ET Nursing Services, Jacksonville
Colon and Rectal Surgery, Reynoldsburg
Cleveland Clinic, Cleveland
Restored Images, Kansas City
Image Specialties, Saint Joseph
University Hospital Freiburg, Freiburg im Breisgau
Private Practice, Tuscon
Homerton University Hospital NHS, London
Chelsea and Westminster Hospital, London
Lead Sponsor
ConvaTec Inc.
INDUSTRY