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Envision® Surface Evaluation | Clinical Trials | Clareo Health

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COMPLETEDNCT00405795

Envision® Surface Evaluation

This observational study will acquire initial clinical practice utilization and product safety data for the Envision® surface.

Lead sponsor: Hill-Rom•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Hill-Rom

This is a single site, open label, observational study to acquire initial clinical practice utilization information, product safety, and wound healing data, as defined by changes in wound volume and/or surface area, for patients with pressure ulcers placed on this surface.

Age

All ages

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Subject Weight \< 400 lbs. Subject has Stage II, III, or IV pressure ulcer on weight bearing aspect of the body Subject estimated length of stay at least 7 days Subject Ability to provide informed consent

Exclusion Criteria

•Inability to provide informed consent

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 4, 2008Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment30

Start dateJun 2007

Last updatedJul 4, 2008

Condition

Locations shown

Levindale Hebrew Geriatric Center and Hospital

Baltimore, Maryland

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 4, 2008Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions