Clinical Trial

Fertility and Ovarian Reserve in Female Childhood Cancer Survivors

Study acronym: PRINCESS
Recruiting
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Summary
Ovarian function impairment affects the quality of life of the survivors of paediatric cancer by impacting fertility, bone quality and mental and cognitive health. The objective of this project is to evaluate the impact of low-intermediate dose alkylating agents associated or not with ovarian cryopreservation technique on ovarian function in female survivors of paediatric cancer. We propose to identify new epigenetic markers in order to predict the risk of premature ovarian insufficiency. The project will be led by a national multi-disciplinary team (paediatric oncologists, gynaecologists, endocrinologists). Paediatric cancer clinical data (therapy, fertility preservation, ...) will be extracted from the Paediatrics Late Effects database and additional data will be collected during PRINCESS fertility evaluation. Through translational and multi-disciplinary approaches, results should improve quality of life and fertility preservation in female survivors of paediatric cancer by developing new personalised screening tools for premature ovarian insufficiency.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-10-02; most recent amendment 2024-10-30.
Status change: Not Yet Recruiting → Recruiting 2024-10-30
Trial Details
NCT Number NCT06626282
Lead Sponsor Centre Hospitalier Universitaire de Liege
Collaborators: La Fondation contre le cancer, Belgique
Conditions Childhood Cancer Survivors, Fertility, Ovarian Reserve, CED, Ovarian Reserve Markers, Cryopreservation, Alkylating Agents, Female
Enrollment 340 participants
Start Date 2024-10-09
Primary Completion 2026-12-31 (estimated)
Study Completion 2028-12-31 (estimated)
Updated on ClinicalTrials.gov 2024-11-01