Clinical trialNCT02389023UnknownInterventional

Comparison of Prevena Negative Pressure Incision Management System vs. Standard Dressing After Vascular Surgery

SponsorUniversity of Vermont Medical CenterEnrollment242ClaudicationCritical Limb IschemiaPeripheral Artery Disease

View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to evaluate the effectiveness of negative pressure incision management system (Prevena™ Incision Management System (PIMS) or ActiVAC® with the Prevena™ Dressings (Peel and Place™ or Customizable™), KCI) in the prevention of wound complications including surgical site infection (SSI) and non-infectious complications in patients undergoing vascular surgery with groin incisions.

clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

Daniel J Bertges, MD
University of Vermont Medical Center
Principal Investigator
clinicaltrials.gov ↗

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States

Maine Medical Center
Portland, Maine, United States
Recruiting
Beth Isreal Deaconess Medical Center
Boston, Massachusetts, United States
Recruiting
Brigham and Women'S Hospital
Boston, Massachusetts, United States
Recruiting
Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, United States
Recruiting
University of Vermont Medical Center
Burlington, Vermont, United States
Daniel Bertges, MD
Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start: 30 Sept 2015
Primary completion: 30 Apr 2019
Completion: 30 Apr 2019
Last update posted: 12 Dec 2018
Registered enrollment: 242
Registry id: NCT02389023

clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.