Actively Recruiting

Age: 18Years +
All Genders
NCT06355245

MEDECA - Markers in Early Detection of Cancer

Led by Danderyd Hospital · Updated on 2024-04-09

1500

Participants Needed

1

Research Sites

456 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Early diagnosis of cancer is key for improving patient outcomes, but cancers are difficult to diagnose if patients present with unspecific symptoms. The principal objective of the MEDECA (Markers in Early Detection of Cancer) study is to identify a multi-analyte blood test that can detect and map occult cancer within a mixed population of patients presenting with serious but unspecific symptoms. The study will include 1500 patients referred to the Diagnostic Center at Danderyd Hospital (DC DS), a multidisciplinary diagnostic center referral pathway for patients with radiological findings suggestive of metastasis without known primary tumor or suspicion of serious but unspecific symptoms. Blood samples are collected prior to a standardized and extensive cancer diagnostic work-up, including an expanded panel of biochemical analyses and extensive imaging such as computed tomography or magnetic resonance investigations. In collaboration with world-leading international scientists, the blood samples will be analyzed for a panel of novel and established blood biomarkers predictive of an underlying cancer, including markers of neutrophil extracellular traps, circulating tumor DNA, platelet mRNA profiling, affinity-based proteomics and nuclear magnetic resonance metabolomics. The diagnostic accuracy of the blood biomarkers with respect to cancer detection during the diagnostic work-up will be analyzed through machine learning.

CONDITIONS

Official Title

MEDECA - Markers in Early Detection of Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age above 18 years
  • Presence of one or more of the following symptoms or signs: general malaise, severe tiredness, unintentional weight loss, fever of unknown cause, uncharacteristic pain lasting more than 4 weeks, abnormal laboratory test results (such as anemia, elevated alkaline phosphatase, erythrocyte sedimentation rate, or calcium), diffuse unexplained pain, marked increase in drug usage, increasing health service seeking behavior, or radiological findings suggestive of metastasis without known primary tumor or suspicion
Not Eligible

You will not qualify if you...

  • Unwillingness to participate in the study
  • Age below 18 years

AI-Screening

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Trial Site Locations

Total: 1 location

1

Danderyd Hospital

Stockholm, Sweden

Actively Recruiting

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Research Team

C

Charlotte Thålin, M.D., Ph.D.

CONTACT

N

Nina Greilert Norin, RN

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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