Clinical Trials Directory

Trials / Unknown

UnknownNCT02499588

User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™

Observational User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™

Status
Unknown
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
ConvaTec Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary aim of this study is to demonstrate the maintenance of healthy peri-stomal skin over a two month period in subjects who use ConvaTec Moldable Technology™ Skin Barriers as part of their standard protocol of care following surgery.

Conditions

Interventions

TypeNameDescription
DEVICEEsteem Plus with ConvaTec Moldable Technology
DEVICENatura with ConvaTec Moldable Technology
DEVICENatura Accordion with ConvaTec Moldable Technology
DEVICEEsteem synergy Plus with ConvaTec Moldable Technology

Timeline

Start date
2015-06-01
Primary completion
2016-08-01
First posted
2015-07-16
Last updated
2015-07-16

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT02499588. Inclusion in this directory is not an endorsement.