Innovative blood tests for ovarian cancer detection
Official title: Multi-site, Multi-country Evaluation of Innovative Ovarian Cancer Biomarker Assays. (DISARM Clinical Study B-CSB)
Run by National and Kapodistrian University of Athens · NCT07693894 · Data updated 2026-11-12
This study tests several blood-based ovarian cancer tests to see if they can distinguish women with ovarian cancer from those without it.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 35 Years and up |
| Sex | Women only |
| Enrollment | 2080 (estimated) |
| Sponsor | National and Kapodistrian University of Athens Academic / other |
| Locations | 7 sites (Prague and 6 other locations) |
| Status | Recruiting |
| Started | August 3, 2026 |
| Main results expected | December 2028 |
| Study ends | December 2028 |
| Registry record updated | October 1, 2026 |
| Trial ID | NCT07693894 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are women aged 35 or older who have epithelial ovarian cancer diagnosed by biopsy or who are healthy controls without cancer and able to consent.
✕Probably not a fit
Patients who do not have ovarian cancer or do not provide adequate samples or consent may not receive any direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This multisite study evaluates investigational liquid biopsy biomarker assays for ovarian cancer, using blood samples from women with EOC and healthy controls. It compares test results to standard blood tests and genetic data to understand relationships with cancer. The design is observational with no randomization or interventions beyond blood collection. Participants include patients with suspected ovarian cancer undergoing surgery or biopsy and healthy controls, with tissue diagnosis used for classification where applicable.
Why it matters
Potential benefit: If successful, the biomarker tests could help identify ovarian cancer earlier or more accurately in the future.
How similar studies have gone: Previous liquid biopsy research in ovarian cancer has shown promising signals but remains exploratory and not yet part of standard care.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: EOC patients 1. Women, trans men and non-binary people with female reproductive organs 2. Aged ≥35 years\* 3. Pathologically diagnosed, by biopsy, with EOC prior to surgical intervention or treatment 4. Presenting with adnexal mass suspicious of OC on imaging and scheduled for surgical resection or biopsy (and subsequent confirmation of EOC) 5. Able to give informed consent Healthy controls 1. Women, trans men and non-binary people with female reproductive organs 2. Aged ≥35 years 3. No cancer history 4. Able to give informed consent Exclusion Criteria: 1. Prior history and any treatment for malignancy 2. Prior removal of either ovary for any reason 3. Pregnant or lactating 4. Any condition or circumstance that, in the opinion of the investigator, could interfere with the participant's ability to participate or comply with study requirements
Where it's running
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Vseobecna Fakultni Nemocnice V Praze
Prague, Czechia Recruiting -
Fakultni Nemocnice Bulovka
Prague, Czechia Recruiting -
National Centre for Scientific Research Demokritos
Athens, Attica, Greece Recruiting -
Dept of Clinical Therapeutics, Alexandra Hospital
Athens, Greece Recruiting -
Instituto Português de Oncologia de Lisboa Francisco Gentil E.P.E.
Lisbon, Portugal Recruiting -
Imperial College Healthcare NHS Trust Hammersmith Hospital
London, United Kingdom Recruiting
Show 1 more location
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Lithuanian University of Health Sciences
Kaunas, Lithuania Not yet recruiting
Study contacts
- Study coordinator: Michael Liontos
- Email: mlionto@med.uoa.gr
- Phone: +302132162845
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.