New study to review egg donor experiences after french law change
NCT ID NCT07468331
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks back at the egg donation process at Nancy University Hospital since France updated its bioethics laws in 2021. Researchers will review the records of about 60 women who started the donation process to see how many completed it and what helped or hindered them. The goal is to find ways to improve the donor experience and increase the number of eggs available for people needing fertility treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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May 2026
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
The study population includes all women evaluated for primary or secondary oocyte donation at Nancy University Hospital during the study period. All candidates who attended a biological consultation and initiated the donation assessment process are included, irrespective of donation completion status.
- Ages
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18 to 38 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All women who attended a biological consultation for primary or secondary oocyte donation at Nancy University Hospital during the study period. Exclusion Criteria: * Absence of biological consultation for oocyte donation during the study period ; * Insufficient or missing medical data ; * Documented opposition to data use for research purposes.
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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University Hospital of Nancy (CHRU Nancy)
Nancy, France
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