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New study tracks fertility and child health in young breast cancer survivors

NCT ID NCT07376681

Knowledge-focused Sponsor: Taizhou Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This observational study follows 2000 women aged 40 or younger with breast cancer to see how having a baby after diagnosis affects their survival and disease return. It also checks the growth and health of their children. The goal is to gather information, not to test a new 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

About 2,000 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

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

Young breast cancer (≤40years)

Ages

18 to 40 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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.

Inclusion Criteria: Only subjects who meet all of the following inclusion criteria can be enrolled in this trial: 1. Female patients diagnosed with breast cancer aged ≤ 40 years; 2. Patients with pathologically confirmed breast cancer, and TNM stage 0-III, the disease is in a stable or progressive state; 3. Complete medical records and clinical follow-up data were available. Informed consent. Exclusion Criteria: Anyone who has one of the following conditions cannot be included in this trial: 1. Female patients with a diagnosis age\>40 years; 2. Stage IV breast cancer at first diagnosis; 3. The presence of other reproductive system diseases caused by oligomenorrhea or amenorrhea and infertility; Loss of clinical data or loss to follow-up.

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Conditions

The condition(s) this trial relates to.

breast cancer breast neoplasm infertility disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breast cancer Fertility Prognosis Young people

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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.

    Open the record ↗

  3. 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

  • Taizhou Central Hosipital

    Taizhou, Zhejiang, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.