Biocollection for infertility research
Medical Assistance for Procreation Patient Library Targeting Patients With Idiopathic Infertility or Low Ovarian Reserve Before the Age of 35
This study is trying to collect health information from people undergoing fertility treatments to help find new ways to understand and improve infertility.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 250 (estimated) |
| Ages | 18 Years to 43 Years |
| Sex | Female |
| Sponsor | University Hospital, Brest Academic / other |
| Locations | 1 site (Brest) |
| Trial ID | NCT05599724 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a biocollection of patients undergoing medically assisted procreation to facilitate future research. It involves multiple consultations where clinical and biological data will be collected, including hormonal assessments and tests for infections. The study seeks to identify new biomarkers and risk factors associated with infertility and to monitor the outcomes of assisted reproductive technology (ART) treatments. Participants will be followed through their treatment cycles and pregnancy if successful.
Who should consider this trial
Good fit: Ideal candidates are women aged 18 to 43 who have been experiencing infertility for at least 12 months and are oriented towards IVF.
Not a fit: Patients who are minors, over 43 years old, or unable to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and treatment of infertility, potentially increasing the chances of successful pregnancies.
How similar studies have performed: Other studies have shown success in identifying biomarkers and risk factors in infertility, making this approach promising but not entirely novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Signed consent * Aged 18 to 43 * Infertility for at least 12 months * Oriented in IVF * Infertility of unexplained origin or presenting a low ovarian reserve before the age of 35 (AMH\<1.1ng and/or CFA\<7). Exclusion Criteria: * Minor patients or \> 43 years old * Patients under guardianship, curatorship (legal protection) * Refusal to participate * Patient unable to consent
Where this trial is running
Brest
- CHRU de Brest — Brest, France (Recruiting)
Study contacts
- Study coordinator: Sarah BOUEE
- Email: sarah.bouee@chu-brest.fr
- Phone: +33 02 98 22 32 22
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.