This trial is terminated!
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Your journey
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More info
You can access this
clinical trial
if you have
Arteriovenous Fistula or Fistula
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

The main objective of this study is to evaluate and compare the primary patency rate at 12 months in a group of hemodialysis patients operated on by cutting balloon and in a group of hemodialysis patients operated by conventional balloon.

Provided treatments

  • Procedure: Cutting balloon angioplasty
  • Procedure: Angioplasty

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: NCT01321866. The sponsor of the trial is Centre Hospitalier Universitaire de Nīmes and it is looking for 42 volunteers for the current phase.
Official trial title:
Randomized Trial Comparing a Cutting Balloon to a Non-cutting Balloon for the Treatment of Venous Stenosis in the Fistulas of Hemodialyzed Patients