CompletedNot Applicable

Male breAsT cAncer preDisposition Factor

France93 participantsStarted 2024-02-08

Plain-language summary

This is a non-interventional, prospective, single-center study designed to collect and describe environmental and psychosocial data from patients with a history of male breast cancer (MBC) referenced in the IUCT-O regional database. The study will be conducted on a population of 110 to 150 patients.

Who can participate

Age range

18 Years

Sex

MALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Male patient with a personal history of breast cancer
. Age ≥ 18 years
. Patient who has had an oncogenetic consultation at IUCT-O and is registered in the IUCT-O oncogenetic database
. Patient for whom no pathogenic variant has been detected on the HBOC panel (HBOC-)
. Patient with no objection to participation in the trial (for deceased patients: trusted support person with no objection to participation).

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

The environmental data in the questionnaire will be described by the usual descriptive statistics.

Timeframe: 15 days for each patient

Psychosocial data from the questionnaire will be described using standard descriptive statistics.

Timeframe: 15 days for each patient

Trial details

NCT IDNCT06219187

SponsorInstitut Claudius Regaud

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-02-06

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