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

ConditionRenal Failure
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

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 criteria

Qualifiers

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;

Disqualifiers

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;

Trial design

Treatments tested in this trial

  • Creation of an arteriovenous fistula

Treatment groups

544 Participants
are divided into 1 treatment group

Sponsors and collaborators