Actively Recruiting
Combination of Data From European Cohorts as Part of the European MORPHEUS Project - MC-MORPHEUS
Led by University Hospital, Brest · Updated on 2026-01-09
20000
Participants Needed
1
Research Sites
287 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The MORPHEUS project is an international research program involving eight European countries, coordinated by France, that aims to improve long-term treatment for unprovoked venous thromboembolic disease (VTED). This research combines clinical, biological, morphological, and socio-anthropological data to create a risk prediction tool to support shared medical decision-making. The MC-MORPHEUS phase focuses on identifying key biomarkers predictive of risks like thromboembolic recurrence, bleeding, and mortality. MC-MORPHEUS collects and merges data from 14 European cohorts into a single database, integrating clinical, biological, and morphological information from patients with venous thromboembolism who have been followed for months or years. This combined dataset will enhance the identification of important biomarkers, which will be used to develop and validate a time-dependent, multi-level risk prediction tool in future studies. Participants in these cohorts have been monitored over long periods, and the study involves processing and analyzing this merged data from late 2024 through 2025. The research will assess consistency between merged and original cohort data and evaluate long-term risks of thromboembolic recurrence, bleeding, and death over 20 years. This observational study does not involve direct interventions but focuses on data analysis and tool development to improve VTED treatment.
CONDITIONS
Brief Title
CoMbination of Data From European Cohorts as Part of the European MORPHEUS Project [HORIZON-HLTH-2022-11-01] - "MC-MORPHEUS".
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cohorts led by members of the European MORPHEUS project consortium
You will not qualify if you...
- Lack of consent in cohorts
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 20 years
Participants from European cohorts with venous thromboembolic disease are observed over several months and years to identify clinical, biological, and morphological biomarkers for risk prediction.
Trial Site Locations
Total: 1 location
1
Chu Brest
Brest, France, 29609
Actively Recruiting
Research Team
F
Francis COUTURAUD
C
Cécile TROMEUR
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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