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Methylation Analyses for Gynaecological Research Through Home-based Self-sampling

RecruitingNAAges 18 Years - anyFemaleUniversiteit Antwerpen
NCT07902388 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of the MARGOT study is to collect self-samples, such as first-void urine and vaginal samples, from people without cancer and compare them with samples from people with gynecological (pre-)cancers collected in other studies, to better understand the differences in biological markers present in these samples between these two groups.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Individuals having female genital organs, regardless of their gender identity * Participant is 18 years or older at the time of signing the informed consent form * Participant must be able to understand the (Dutch) information consent form and what the study is about * Participant must be able to provide written informed consent and take urine- and vaginal self-samples * Individual has a Belgian nationality Exclusion Criteria: * Individuals that underwent hysterectomy or ovariectomy * Pregnant individuals or 6 months post-partum * (History of) (pre)cancer, or an ongoing diagnostic work-up or treatment for oncological concerns * Unable to give informed consent or to take urine- or vaginal self-samples * Participation in another interventional study. However, participation in another low-interventional or observational study is allowed * Individuals who have (a history) of postmenopausal bleeding
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What it tests

  • Colli-Pee 20 mL device with UCM
  • Evalyn Brush
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Where

1 site
University of Antwerp, Center for the Evaluation of Vaccination, Vaccinopolis
Edegem, Belgium
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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