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Infertility,FemaleNCT06529224

Social Egg Freezing: Will Health Professionals Offer it ?

An observational study of Infertility,Female, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In 2021, the revision of bioethics laws opened the door to elective egg freezing. This gives women, between their 29th and 37th birthdays, the opportunity to freeze their eggs in order to combat age decline fertility. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Infertility,Female
What is being tested?
Online questionnaire
How many people
1,551 participants
Where
1 siteFrance
Study dates
5 Apr 2024to 30 Oct 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Practising GPs, gynaecologists or midwives

Who may be able to join

  • Be a general practitioner, gynecologist or midwife in practice for at least one year
  • Follow patients between 29 and 37 years old (for their contraception for example)

Who cannot join

  • Have been practising for less than a year
  • Have no patients aged between 29 and 37

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU Saint Etienne

    Saint-Etienne, 42000

Other trials in France

About this study

In 2021, the revision of bioethics laws opened the door to elective egg freezing. This gives women, between their 29th and 37th birthdays, the opportunity to freeze their eggs in order to combat age decline fertility. However, communication about this new possibility has remained limited both toward women and their health professional.

Read the detailed description

Thus, the hypothesize of this study is that these professionals, namely physicians, gynecologists and midwives, are insufficiently aware of age-related fertility decline and unaware of the possibility of elective egg freezing.

This multicenter observational cross-sectional study whose objective will be:

  • To assess the knowledge of these professionals in terms of age-related fertility decline.
  • To measure their propensity to spontaneously broach the subject with their childless patients.
  • To assess their knowledge and support for elective egg freezing. This study will be done using an online questionnaire that will be distributed in electronic format to all the health professionals concerned in the participating areas.

This study will provide valuable knowledge on the perception of elective egg freezing by health professionals, determine their training needs and motivate new information campaigns on this subject.

Being tested
Online questionnaire
Keywords
Elective egg freezing, Attitude of health professionals, Health knowledge, Aging, Female infertility
Medical subject headings
Infertility, Female

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Online questionnaireOther

    An online questionnaire will be distributed in electronic format to all the healthcare professionals concerned.

Study groups in NCT06529224
Study groupRoleWhat they receive
Health professionalsGeneral practitioner, gynecologist or midwife
Receives: Other: Online questionnaire

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Knowledge of primary care professionals regarding age-related decline in fertility.

    Analysis questionnaire results.

    Measured: Day 1

  2. Propensity to spontaneously broach the subject with their patients without children.

    Analysis questionnaire results.

    Measured: Day 1

  3. Knowledge and support for the elective egg freezing.

    Analysis questionnaire results.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Jul 2024
  2. Study start5 Apr 2024
  3. Primary completion30 Oct 2024
  4. Study completion30 Oct 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
1,551 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06529224
Sponsor's protocol ID
IRBN942023/CHUSTE
Status last verified
Oct 2026
First submitted
26 Jul 2024
Last updated
16 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Infertility,Female, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Knowledge of primary care professionals regarding age-related decline in fertility. (time frame: Day 1). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2026.

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