Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06815159

Tissue Markers Predictive of Early Stenosis in the Arterovenous Fistula for Hemodialysis

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-02-07

150

Participants Needed

1

Research Sites

302 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study involves the recruitment of two populations. POPULATION 1 (surgical sample of excess venous segment): at least 75 consecutive patients, enrolled according to the inclusion criteria and subjected to first AVF surgery as part of the normal care pathway, at the Metropolitan Vascular Surgery Unit, Dir. Prof. Mauro Gargiulo of the S.Orsola-Malpighi University Hospital. POPULATION 2 (surgical sample of arterialized venous segment from removal of previous AVF): at least 75 consecutive patients, enrolled according to the inclusion criteria and subjected to reoperation for correction of complication and/or new AVF by proximalization, as part of the normal care pathway, at the Metropolitan Vascular Surgery Unit, Dir. Prof. Mauro Gargiulo of the S.Orsola-Malpighi University Hospital.

CONDITIONS

Official Title

Tissue Markers Predictive of Early Stenosis in the Arterovenous Fistula for Hemodialysis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than or equal to 18 years
  • Patients candidates for first AVF for hemodialysis or correction of AVF complication, as part of the normal care pathway
  • Obtaining informed consent signed by the patient
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

IRCCS AOU di Bologna Policlinico di Sant'Orsola

Bologna, Italy, 40138

Actively Recruiting

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Research Team

M

Mauro Gargiulo, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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