CRISTEL Study: Monitoring of Pregnancies in Women After Solid Organ Transplantation

Starting soon · Not applicable

Conditions studied: Surgical Operation With Transplant of Whole Organ

In brief

The objective of this research is to obtain standardized and independent data on the number of pregnancies occurring in France and their follow-up up to 1 year postpartum (or post-pregnancy termination). This study will then aim to describe the clinical characteristics and maternal and perinatal outcomes of pregnancies in this specific population. These data will enable the dissemination of clear and up-to-date information to the medical community, thus contributing to better patient counseling and, more broadly, to couples. They will also serve to issue recommendations to optimize the planning and follow-up of pregnancies in women with solid organ transplants. Finally, this initiative aims to promote clinical research on pregnancies.

Key facts

Study ID

NCT07592806

Run by

Hopital Foch

People needed

2000

Starts

2026-09-01

Expected to finish

2036-09-01

Last updated by the study team

2026-05-18

Who can join

Age: 18 and older, up to 48. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female patient aged 18 years or older and of childbearing age
• Has received a solid organ transplant, either isolated or combined (heart, liver, lung, pancreas, kidney)
• Has a positive blood beta-hCG test result > 5 IU/L ("positive")
• Has signed an informed consent form
• Affiliated with a health insurance plan

You may not qualify if…

• Patient deprived of liberty or under legal guardianship
• Patient refuses to participate in the study

Full record on ClinicalTrials.gov

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