NCT06626282Recruiting
Fertility and Ovarian Reserve in Female Childhood Cancer Survivors
PReserving Fertility and Quality of Life IN Belgian Female Paediatric CancEr SurvivorS
Source: ClinicalTrials.gov · Last updated 1 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 340 (estimated)
- First submitted
- 2 Oct 2024
- Start date
- 9 Oct 2024
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Centre Hospitalier Universitaire de Liege
- Diseases
- Ovarian cancer
- NCT number
- NCT06626282
What you commit to
- Study type: Observational
- Planned participants: 340
- From 9 Oct 2024 to the primary completion date, 31 Dec 2026
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Cancer diagnosis for controls
Who the study is looking for
- Child and adolescent female patients included in the Paediatrics Late Effects Project:
- diagnosed with cancer1 between 01/01/2004 and 31/12/2018
- \<17 years old at diagnosis
- treated at CHU Liège site Citadelle or CHC, Cliniques Universitaires Saint-Luc and HUDERF
- alive
- ≥ 18 years-old at time of recruitment.
Age in the registry: 18 years to 50 years · Sex: Female · Accepts healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| HUDERF Coordinator of this site? Confirm its status | Brussels | Belgium | Not yet recruiting |
| Cliniques universitaires Saint-Luc Coordinator of this site? Confirm its status | Brussels | Belgium | Not yet recruiting |
| Hôpital de la Citadelle Coordinator of this site? Confirm its status | Liège | Belgium | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.