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 @ 11:54 PM
Ignite Modification Date:
2025-12-24 @ 11:54 PM
NCT ID:
NCT03076151
Eligibility Criteria:
Inclusion Criteria:
1. Subject's written informed consent of the study
2. Male and female (\>= 18 years)
3. Recipients of a first kidney allograft
4. Patients transplanted for less than 7 days at enrolment
5. Patients affiliated to a social security system
Exclusion Criteria:
1. Patients presenting any contraindication to tacrolimus according to the summary of product characteristics of Adoport®
2. Patient presenting anti-HLA antibodies against the graft in pre-transplantation (DSA)
3. Recipients of any transplanted organ other than the kidney
4. Pregnant (positive BHCG test) or lactating women
5. Women without any method of contraception, except for women with no childbearing potential (according to the guidelines of the working group, Clinical Trial Facilitation Group, related to contraception and pregnancy test in clinical trials)
6. Patients participating in any other interventional clinical study at inclusion as well as during the whole course of the current study
7. Patient under judicial protection
8. Patients incapable of understanding the purposes and risks of the study, who cannot give written informed consent, or who are unwilling to comply with the study protocol
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03076151
Study Brief:
Protocol Section:
NCT03076151