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NCT06889844Recruiting

Observational Cross-reactivity Study for Colorectal Cancer Diagnosis

Observational Cross-reactivity Study to Evaluate the Specificity of a Blood Test for Colorectal Cancer Diagnosis Based on Molecular Markers and Risk Factors Identified With Artificial Intelligence Tools

Source: ClinicalTrials.gov · Last updated 1 Oct 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The objective of this observational study is to evaluate the false positive rate of the blood test based on molecular biomarkers and risk factors. A total of 250 patients diagnosed with various cancers and gastrointestinal diseases will be enrolled. The main question to be answered is Does the blood test have a low false positive rate in the main study population? Participants will donate a blood sample as part of their regular medical care for cancer diagnosis and give the consent to know their clinical risk factors.

Status (registry)
Recruiting
Study type
Observational
Enrollment
250 (estimated)
First submitted
17 Mar 2025
Start date
17 Apr 2023
Primary completion date
31 Dec 2025
Lead sponsor
ADVANCED MARKER DISCOVERY S.L.
NCT number
NCT06889844

What you commit to

  • Study type: Observational
  • Planned participants: 250
  • From 17 Apr 2023 to the primary completion date, 31 Dec 2025
  • 5 sites in 1 country
  • 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

  • Patients who have received previous chemotherapy or radiotherapy.
  • In case of diagnosis of a tumor: patients who have undergone total or partial surgical resection of the tumor.

Other illness

  • Patients with a personal history of advanced or non-advanced colorectal adenoma, serrated lesions, colorectal cancer, familial adenomatous polyposis or Lynch syndrome.

Other

  • Patients without appropriate staging or diagnosis.
  • Patients with hemolyzed plasma.

Who the study is looking for

  • Patients older than 18 years of age at the time of blood sample collection.
  • Subjects must be able to understand the information provided on the participant information sheet, must consent to participate in the study, and must sign the informed consent form.
  • Patients diagnosed with only one type of cancer (no colorectal cacner) or gastrointestinal disease.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Universitario HM Sanchinarro
Coordinator of this site? Confirm its status
MadridSpainRecruiting
MD Anderson Cancer Centre
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting
Hospitales HM de Malaga
Coordinator of this site? Confirm its status
MálagaSpainRecruiting
Hospital Universitario de Ourense
Coordinator of this site? Confirm its status
OurenseSpainRecruiting
Hospital Centro Médico Asturias
Coordinator of this site? Confirm its status
OviedoSpainRecruiting

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