RecruitingNCT06297343

Study of the Risk of Ischaemia Following the Creation of an Arteriovenous Fistula


Sponsor

GCS Ramsay Santé pour l'Enseignement et la Recherche

Enrollment

544 participants

Start Date

Oct 20, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to identify functional vascular changes and clinical factors correlated with the occurrence of short- or medium-term hand ischaemia after arteriovenous fistula creation.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Creation of an arteriovenous fistula for people with renal failure. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURECreation of an arteriovenous fistula

Patients will undergo the surgical procedure to create an arteriovenous fistula and will be discharged the same day (outpatient care, or an overnight stay in hospital if they live a long way from the hospital, have multiple pathologies or are socially isolated). An arteriovenous fistula is created under local or general anaesthetic. On the day of the operation, the type of arteriovenous fistula created, the side of the arteriovenous fistula, the location of the arteriovenous fistula and the patency of the arteriovenous fistula will be collected.


Locations(1)

Hôpital Privé des Peupliers

Paris, France

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NCT06297343


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