Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT05096351
Eligibility Criteria:
Inclusion Criteria:
* The patient must be a member or beneficiary of a health insurance plan
* Patients receiving a scheduled venous allograft within the CHU of Nîmes for an arterial bypass in the lower limb or an arteriovenous bypass in the upper limb within the framework of the creation of arteriovenous fistulas in dialysis patients, in the absence of available autologous venous material.
Exclusion Criteria:
* The subject is participating in a category 1 interventional study, or is in a period of exclusion determined by a previous study
* The subject has already been included in the study
* The subject refuses to participate
* It is impossible to give the subject informed information
* The patient is under safeguard of justice or state guardianship
* Patient previously having received a venous allograft or organ transplant
* Pregnant, parturient or breastfeeding patients
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05096351
Study Brief:
Protocol Section:
NCT05096351