Genome-based Management of Patients in Precision Medicine (Ge-Med) Towards a Genomic Health Program
University Hospital Tuebingen
12,000 participants
Jun 1, 2021
INTERVENTIONAL
Conditions
Summary
The GE-MED APPROACH project will enroll patients (n = appr. 12.000) with unclear molecular cause of the disease, suspected genetic cause of the disease without detailed molecular analysis like Whole Exome Sequencing (WES). The novelty of this study is to integrate genomic health concepts into immediate clinical care. To achieve these goals, a novel structure for the Triple P (3P) concept of personalized medicine (Personalized, Predictive, Preventive) integrated into a well-established health care system and associated with novel decentralized Disease Analysing Task Forces (DATF) will be implemented. The overall goal of this study is to implement, for the first time, Whole Genome Sequencing (WGS) analysis as a first line diagnostic test for all clinical indications such as Rare Disease (RD )and familial cancer syndromes.
Eligibility
Inclusion Criteria2
- Unclear molecular cause of the disease
- Suspected genetic cause of the disease
Exclusion Criteria2
- Missing informed consent of the patient and if applicable the legal representative
- Previously performed WES or panel analysis
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Interventions
Blood sampling, short clinical characterization, WGS based sequencing, NGS analysis and other omics analysis (transcriptomics, proteomics, metabolomics).
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04760522