Study of the Risk of Ischaemia Following the Creation of an Arteriovenous Fistula
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
France
Hôpital Privé des Peupliers
RECRUITING
Paris
Contact Information
Primary
Viviane DUEDAL, MD
v.duedal@gmail.com
6 70 80 18 98
Time Frame
Start Date: 2025-10-20
Estimated Completion Date: 2027-12
Participants
Target number of participants: 544
Treatments
Adult patients with chronic renal failure
Adult patients with chronic renal failure for whom arteriovenous fistula creation is planned
Related Therapeutic Areas
Sponsors
Leads: GCS Ramsay Santé pour l'Enseignement et la Recherche
Collaborators: Euraxi Pharma