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

NCT01354899 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2016-05-09

Study results available
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Summary

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.

Conditions

  • Critical Illness

Sponsors & Collaborators

  • Molnlycke Health Care AB

    lead INDUSTRY

Principal Investigators

  • Jan Faergemann, Professor · Dermatology Department Sahlgrenska University Gothenburg

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01354899 on ClinicalTrials.gov