University Hospital Tuebingen: Rare Diseases trials

The registry lists 10 Rare Diseases studies with University Hospital Tuebingen as lead sponsor. 7 are open to participants now and 0 have results posted.

No phase 10(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• Rare Tumours in Children and Adolescents (STEP)RecruitingNCT05773651
• Genome-based Management of Patients in Precision Medicine (Ge-Med) Towards a Genomic Health ProgramRecruitingNCT04760522Not applicable
• Diagnostic Value of Exome/ Genome Sequencing, Conventional Methods in Rare Diseases and Familial Tumor SyndromesRecruitingNCT04731857
• European Registry on Rare Neurological DiseasesNot yet recruitingNCT04319796
• Identification of the Genetic Causes of Rare Diseases With Negative Exome FindingsRecruitingNCT04315727Not applicable
• Genetic Causes of Discrepant Clinic in Monogenic TwinsRecruitingNCT04046796
• Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare DiseasesRecruitingNCT03491280
• Mitochondrial Diseases - Long-read Genome and Transcriptome Sequencing in Cases Unresolved After Short-read GenomicsCompletedNCT03962452Not applicable
• Whole Genome Trio Sequencing as a Standard Routine Test in Patients With Rare Diseases - "GENOME FIRST APPROACH"CompletedNCT03954652Not applicable
• Next Generation Sequencing Diagnostics - On the Road to Rapid Diagnostics for Rare DiseasesStatus unknownNCT02588638