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NCT04539015

Assess the Efficacy of Prevena Plus vs SOC to Closed Incision in Pts Undergoing CAWR and Other Laparotomy Procedures.

Status unknown Last updated 4 September 2020
What this trial tests

trial testing Prevena Plus in Hernia in 170 participants. Status unknown.

Timeline
9 July 2020
Primary endpoint
30 December 2022
28 February 2023

Quick facts

Lead sponsorNew York Medical College
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment170
Start date9 July 2020
Primary completion30 December 2022
Estimated completion28 February 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

New York Medical College

Who can join

18 and older, any sex, with Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this study to establish the efficacy of Prevena™ Plus in preventing surgical site infection after complex abdominal wall procedures and major laparotomies as compared to SOC dressing. We hypothesized that use of Prevena Plus will significantly decrease the incidence of Surgical Site Infection (SSI) and subsequently may have an impact over reducing hospital cost. Study data will be analyzed for clinical outcomes through 30 days. The patients will be followed every day during the hospital stay and study follow-up visits will be conducted in the clinic at 2 weeks and 1 month from the date of discharge.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Negative pressure wound therapy for surgical wounds healing by primary closure.
    Norman G, Shi C, Goh EL, Murphy EM, et al · · 2022 · cited 71× · PMID 35471497 · DOI 10.1002/14651858.cd009261.pub7

Verify or expand the search:

Other recruiting trials for Hernia

Currently open trials in the same condition.

Other New York Medical College trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04539015.

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