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NCT07693894Recruiting

Innovative Ovarian Cancer Biomarker Assays

Multi-site, Multi-country Evaluation of Innovative Ovarian Cancer Biomarker Assays. (DISARM Clinical Study B-CSB)

Source: ClinicalTrials.gov · Last updated 1 Oct 2026

Brief summary (registry, in English)

Ovarian cancer is often diagnosed at a later stage because early symptoms can be mild or non-specific. Earlier detection of ovarian cancer could improve treatment options and outcomes. Recent research has focused on the development of blood-based tests, sometimes referred to as liquid biopsy tests, which aim to look for changes in the blood that could be linked to cancer. These tests are still under investigation and are not part of routine clinical care. The purpose of this study is to evaluate several blood-based ovarian cancer tests. This will be done by comparing test results from people who have ovarian cancer with results from people who do not have cancer. The study will also collect information from standard blood tests and genetic analyses to better understand how these results relate to ovarian cancer. This study is for research purposes only. The blood-based tests being evaluated are investigational and are not used to make medical decisions or diagnoses for women taking part in the study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2080 (estimated)
First submitted
5 Jul 2026
Start date
3 Aug 2026
Primary completion date
Dec 2028
Lead sponsor
National and Kapodistrian University of Athens
NCT number
NCT07693894

What you commit to

  • Study type: Observational
  • Planned participants: 2080
  • From 3 Aug 2026 to the primary completion date, Dec 2028
  • 7 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior history and any treatment for malignancy
  • Prior removal of either ovary for any reason

Other illness

  • 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

Other

  • Pregnant or lactating

Who the study is looking for

  • EOC patients
  • Women, trans men and non-binary people with female reproductive organs
  • Aged ≥35 years\*
  • Pathologically diagnosed, by biopsy, with EOC prior to surgical intervention or treatment
  • Presenting with adnexal mass suspicious of OC on imaging and scheduled for surgical resection or biopsy (and subsequent confirmation of EOC)
  • Able to give informed consent
    • Healthy controls
  • Women, trans men and non-binary people with female reproductive organs
  • Aged ≥35 years
  • No cancer history
  • Able to give informed consent

Age in the registry: 35 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Fakultni nemocnice Bulovka
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PragueCzechiaRecruiting
Vseobecna fakultni nemocnice v Praze
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PragueCzechiaRecruiting
Imperial College Healthcare Nhs Trust - Hammersmith Hospital
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LondonUnited KingdomRecruiting
Dept of Clinical Therapeutics, Alexandra Hospital
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AthensGreeceRecruiting
National Centre for Scientific Research Demokritos
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AthensGreeceRecruiting
Lithuanian University of Health Sciences
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KaunasLithuaniaNot yet recruiting
Instituto Portugues de Oncologia de Lisboa Francisco Gentil, E.P.E.
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LisbonPortugalRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.