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Fabric
DermaTherapy® Linen group for Pressure Sores
N/A
Waitlist Available
Led By Kenneth E Schmader, MD
Research Sponsored by Precision Fabrics Group, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up weekly for 8 weeks
Awards & highlights
Study Summary
The primary purpose of this research study is to evaluate if DermaTherapy® bedding will significantly reduce pressure ulcer incidence by decreasing maceration, friction, and shearing among residents of Nursing Homes.
Eligible Conditions
- Pressure Sores
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ weekly for 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~weekly for 8 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Prevention and reduction in the incidence of pressure ulcers
Secondary outcome measures
Reduction of bacterial contamination
Trial Design
1Treatment groups
Experimental Treatment
Group I: DermaTherapy® Linen groupExperimental Treatment1 Intervention
The DermaTherapy® Linen group uses bed sheets and underpads made with DermaTherapy® fabric.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
DermaTherapy® Linen and underpads.
2010
N/A
~80
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Who is running the clinical trial?
Precision Fabrics Group, Inc.Lead Sponsor
3 Previous Clinical Trials
3,458 Total Patients Enrolled
US Department of Veterans AffairsFED
868 Previous Clinical Trials
487,815 Total Patients Enrolled
Kenneth E Schmader, MDPrincipal InvestigatorDurham VA medical Center, Duke University Medical Center
1 Previous Clinical Trials
75 Total Patients Enrolled
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