AMH and Hormonal Profiles in Women with Breast Cancer

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects AMH, FSH, estradiol, TSH, and fT4 from women aged 20-55, including breast cancer patients at various treatment stages and healthy controls. For breast cancer participants, tests proceed as part of usual care without extra procedures; data are gathered from medical records. Healthy volunteers provide a single blood sample and answer a brief questionnaire. The goal is to describe hormonal profiles and assess the feasibility of incorporating AMH testing into routine clinical practice, with preliminary data to inform future research.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Women aged 20-55 years.
* Patients with a diagnosis of breast cancer at any of the specified stages of treatment or follow-up, or healthy female volunteers.
* Blood sampling as part of routine clinical care (breast cancer patients) or willingness to undergo a single blood draw (healthy volunteers).

Exclusion Criteria:

* Inability or unwillingness to participate in the study.

Where it's running

• Masaryk Memorial Cancer Institute
  Brno, Czechia Recruiting

Study contacts

• Study coordinator: Iveta Selingerova, Ph.D.
• Email: iveta.selingerova@mou.cz
• Phone: +420543136720

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.