A Open Study to Evaluate the Performance of Dressing on Subject With High Risk of Skin Breakdown

Molnlycke Health Care

Status: Completed

Conditions: Critical Illness

Study type: Observational

Funder types: Industry

Identifiers

NCT01354899

WINDOW 01

Window 02

Details and patient eligibility

About

The rational for the study is to add a thin self-adherent dressing on critically ill patients. Evaluate if the dressing might protect the skin for further breakdown.Participants will be followed for the duration of hospital stay, an expected average of 5 days.

Enrollment: 24 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Provision of written informed consent
• Braden total score ≤ 12 at enrolment
• Male or female, ≥ 18 at enrolment
• No skin- breakdown
• Subject or family member is able to understand and comply with the requirements of the study, judged by the investigator

Exclusion criteria

• Risk area dosen´t fit the dressing size
• Documented skin disease
• Kown allergy to any of the components in the dressing
• Previous enroled in present study
• Subject included in other ongoing clinical investigation