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