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Clinical trial

Retrospective Cohort Study Assessing the Natural Course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and Sporadic and Hereditary Inclusion Body Myopathies (IBM)

NCT01902940 is registered in ClinicalTrials.gov with Ludwig-Maximilians - University of Munich as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Retrospective Cohort Study Assessing the Natural Course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and Sporadic and Hereditary Inclusion Body Myopathies (IBM)
Lead sponsor
Ludwig-Maximilians - University of Munich
Phase
Observational
Overall status
Completed
Start date
June 30, 2013
Completion date
October 31, 2013
Enrollment
350 (actual)
Sites
1

Conditions

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

congenital cataracts, facial dysmorphism, and neuropathy, inclusion body myopathy, autosomal-dominant, inclusion body myopathy, autosomal-recessive, inclusion body myositis, sporadic