Actively Recruiting
Study of the Risk of Ischaemia Following the Creation of an Arteriovenous Fistula
Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2025-11-24
544
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
Sponsors
G
GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead Sponsor
E
Euraxi Pharma
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Study of the Risk of Ischaemia Following the Creation of an Arteriovenous Fistula
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 informed and has given oral non-opposition to participate
You will not qualify if you...
- Contraindication to the proposed surgery
- Reduced life expectancy as judged by the investigator
- Medical or biological conditions affecting study results or patient safety
- Patient uncooperative or unable to attend scheduled visits
- Other surgical or medical interventions planned during the study
- Pregnant, breastfeeding, or likely to be pregnant without effective contraception
- Participating in another clinical trial or within exclusion period
- Patient under guardianship or deprived of liberty
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital Privé des Peupliers
Paris, France, 75013
Actively Recruiting
Research Team
V
Viviane DUEDAL, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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