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Your journey
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More info
You can access this
clinical trial
if you have
Wound Infection
and you are
The primary goal of this phase is to monitor the long-term effects.
The treatment is already on the market.
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The purpose

All patients with deep venous obstruction below the sapheno-femoral junction elective for hybrid procedure with creation of an arterio venous-fistula (AVF) in the MUMC or patients with primary percutaneous procedure (and thus venous obstruction above the sapheno-femoral junction) who present with occluded stents which need an additional AVF after thrombolysis will receive a Prevena NPWT. Incidence of wound infections and wound scoring will be performed afterwards.

Provided treatments

  • Device: Prevena, KCI, Acelity, NPWT

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02905955. The sponsor of the trial is Maastricht University Medical Center and it is looking for 40 volunteers for the current phase.
Official trial title:
Negative Pressure Wound Management (NPWT) System for Inguinal Wounds After Venous Hybrid Procedures