New biobank aims to unlock secrets of infertility and pregnancy
NCT ID NCT07265908
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is creating a biobank—a collection of blood samples and health data—to help researchers better understand gynecological disorders, infertility in men and women, and pregnancy-related conditions. Up to 3,000 participants will provide samples at San Raffaele Hospital in Milan. The goal is to support future scientific discoveries, not to test any treatment or intervention.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Dec 2043
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
REPRO-Biobank anticipates the enrollment of approximately 300 individuals annually, comprising adult and pediatric patients diagnosed with gynecological disorders, male or female infertility, or pregnancy-related conditions, currently under care at the Gynecology and Obstetrics Unit / Centro Scienze della Natalità of San Raffaele Hospital, as well as healthy volunteers associated with the same Unit.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
1. Affected participants Inclusion Criteria for adult patients (including pregnant and breastfeeding women) and pediatric patients affected by: * Male infertility * Female infertility * Gynecological disorders * Pregnancy-related conditions * Conditions requiring fertility preservation treatment (oocyte cryopreservation, ovarian tissue preservation) * Informed consent signed by the adult patient or by the parents/legal guardians of pediatric patients Exclusion Criteria * Patients unable or unwilling to sign the informed consent 2. Healthy participants Inclusion Criteria * Healthy adult subjects (including pregnant and lactating women) * Able to give informed consent for participation in the study Exclusion Criteria * Patients unable or unwilling to sign the informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Irccs San Raffaele Hospital
Milan, Milan, 20132, Italy
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