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A Pilot Study of the Envision® Surface

H

Hill-Rom

Status

Completed

Conditions

Pressure Ulcers

Treatments

Device: Envision® Patient Support System

Study type

Observational

Funder types

Industry

Identifiers

NCT00405834
CR-0065

Details and patient eligibility

About

This study is to evaluate the clinical safety and effectiveness of the Envision® surface.

Full description

This study is to evaluate the clinical safety and effectiveness of the Envision® surface placed on the TotalCare® frame in pressure ulcer prevention and management, patient comfort, and staff acceptance in the critical care environment

Enrollment

30 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject weighs between 70 and 400 pounds Subject to remain on Envision Surface for at least 3 days Subject at risk for pressure ulcers (Braden Score < 14) or has existing ulcer of any stage Subject is able to provide voluntary consent

Exclusion criteria

  • Subject requires pulmonary treatment surface Subject declines consent

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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