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Single-Use Negative Pressure Wound Therapy for Surgical Incisions
N/A
Waitlist Available
Research Sponsored by Rothman Institute Orthopaedics
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 90-day followup following revision surgery
Awards & highlights
Study Summary
The primary aim of this study is to determine if the SSI rate following revision total hip and knee arthroplasty is reduced in patients treated with the PICO device compared to patients with traditional postoperative dressings. Our secondary goals include; comparing the amount of wound drainage, rate of resolution of wound drainage, length of hospital stay, functional outcomes, and economic implications of wound drainage and SSI after revision arthroplasty comparing PICO and traditional dressings.
Eligible Conditions
- Surgical Incisions
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90-day followup following revision surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90-day followup following revision surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Surgical Site Infection
Trial Design
2Treatment groups
Active Control
Group I: Single-Use Negative Pressure Wound TherapyActive Control1 Intervention
Group II: Standard of CareActive Control1 Intervention
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Who is running the clinical trial?
Rothman Institute OrthopaedicsLead Sponsor
121 Previous Clinical Trials
21,084 Total Patients Enrolled
Frequently Asked Questions
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