VAC GranuFoam Bridge Dressing for Foot Ulcer

N/A

Waitlist Available

Research Sponsored by KCI USA, Inc

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 48-72 hours (+6 hours) time period

Awards & highlights

No Placebo-Only Group

Summary

The study is aimed at evaluating the clinician's perceived ease of using the V.A.C. GranuForm bride dressing and the patients perceived level of comfort during the dressing wear.

Eligible Conditions

Foot Ulcer

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 48-72 hours (+6 hours) time period

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~48-72 hours (+6 hours) time period

This trial's timeline: 3 weeks for screening, Varies for treatment, and 48-72 hours (+6 hours) time period for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Ease of Use Assessment

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups

Experimental Treatment

Group I: VAC GranuFoam Bridge DressingExperimental Treatment1 Intervention

This is a medical device foam dressing allowing placement away from wound site. It is designed to simplify the bridging application. It is used in combination with the V.A.C. Negative Pressure Wound Therapy System. For each subject, the dressing was applied in compliance with the IFU for 48-72 hours.

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

V.A.C. Negative Pressure Wound Therapy System

2009

N/A

~40

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