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Clinical trial

Study of the Familial Phenotype Associated With Mutations in the COL4A1 and COL4A2 Genes

NCT07374913 is registered in ClinicalTrials.gov with Meyer Children's Hospital IRCCS as lead sponsor.

NCT NCT07374913
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Registry record

As filed in ClinicalTrials.gov.

Title
Study of the Familial Phenotype Associated With Mutations in the COL4A1 and COL4A2 Genes
Lead sponsor
Meyer Children's Hospital IRCCS
Phase
Not applicable
Overall status
Recruiting
Start date
May 1, 2021
Completion date
December 31, 2026
Enrollment
120 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

col4a1-related brain small vessel disease with haemorrhage, col4a1\2