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Active, not recruiting Not applicable

Follow-up of Sequential Chemotherapy and Stimulation for Fertility Preservation in Young Patients With Breast Cancer

NCT03795246 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2018-04-12
Last updated
2026-03-18

Condition(s) studied

Breast Cancer

Investigational drug(s) / intervention(s)

ConsultationBiological TestPelvic Ultrasound

Consultation: Consultation in oncology: collection of oncological data and ongoing cancer treatments, clinical exam Consultation in gynecology: collection of gynecological data, contraception and reproductive medicine

Biological Test: Blood test: * FSH, LH, E2 and AMH * 4 tubes of 7 mL

Pelvic Ultrasound: Antral Follicles Count

Study summary

Interventional research with low risks and constraints, prospective and monocentric on the assessment of long-term fertility in patients who underwent an adjuvant sequential chemotherapy with or without a controled ovarian hyperstimulation. This study follows a previous one called NCT 01614704.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients included in the study CT 01614704 * Informed and written consent * Affiliated to the National Social Security System Exclusion Criteria: * Impossibility to submit at the study procedures due to geographic, social or mental reasons * Patient deprived of their liberty or under guardianship or tutorship.

Primary outcome measure(s)

  • Assessment of fertility in terms of cumulative incidence of long-term pregnancy — 10 years after chemotherapy
    for patients who underwent adjuvant sequential chemotherapy of anthracycline and taxane separately, depending on whether or not they have had Controlled Ovarian Hyperstimulation

Trial sites (1)

FacilityCityRegionStatus
Centre Oscar Lambret Lille France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03795246 on ClinicalTrials.gov ↗ ← All trials in France