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

Recruiting now

Conditions studied: Renal Failure

In brief

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.

Key facts

Study ID

NCT06297343

Run by

GCS Ramsay Santé pour l'Enseignement et la Recherche

People needed

544

Starts

2025-10-20

Expected to finish

2027-12-01

Last updated by the study team

2025-11-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years;
• Stage 5 chronic kidney disease, on dialysis or not on dialysis;
• Requiring the creation of an arteriovenous fistula;
• Membership of a social insurance scheme;
• Patient having been informed and having formulated his/her oral non-opposition to participate in the research.

You may not qualify if…

• Contraindication to the proposed surgery ;
• Reduced life expectancy in the opinion of the investigator;
• Medical or biological conditions which, in the opinion of the investigator, could influence the interpretation of the results of the study or the safety of the patient;
• Patient uncooperative with protocol requirements or unable to attend scheduled visits to the centre;
• Other surgical or medical intervention planned during the study;
• Pregnant or likely to be pregnant (of childbearing age, without effective contraception) or breastfeeding;
• Participating in another clinical trial, or in a period of exclusion from another clinical trial;
• Patient under guardianship or deprived of liberty.

Where it is running

• Hôpital Privé des Peupliers — Paris, France (enrolling)

Full record on ClinicalTrials.gov

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