Clinical- and Omic- Based Analysis of Trajectory for COVID-19 Infection and Recovery (COMBATC19IR)
- Funded by Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
- Total publications:1 publications
Grant number: 01KI20249
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Key facts
Disease
COVID-19, UnspecifiedStart & end year
20202021Known Financial Commitments (USD)
$578,425.13Funder
Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)Principal Investigator
Dr. Anne HilgendorffResearch Location
Germany, United States of AmericaLead Research Institution
Helmholtz Zentrum MünchenResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Prognostic factors for disease severity
Special Interest Tags
Innovation
Study Type
Clinical
Clinical Trial Details
Not applicable
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
We aim to develop and validate Artificial Intelligence (AI) models that can reliably predict the course of COVID-19 progression and its complications via: 1) modeling patients clinical trajectories to understand their recovery and potential development of pulmonary complications, 2) characterizing diversity and virulence of the co-infecting viral and microbial community to understand disease mechanisms and severity, and 3) analyzing the host's biological makeup to understand the individual susceptibility to infections in low and high-risk individuals with pre-existing lung conditions. We validate and inform our AI models by clinical datasets and bio-samples collected from five different international patient cohorts: three cohorts in Munich and two in the USA. In addition, we track the COVID-19 patients for their post discharge health status focusing on lung related outcome measures at 3 months to confirm the recovery trajectory observed during hospitalization and compare their disease course and outcome to those recovering from similar-symptom diseases such as Influenza and community-acquired pneumonia. Based on the results obtained by our study, we develop a decision support system for physicians to allocate resources and to plan individualized follow-up care for at-risk patients.
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