Trials / Completed
CompletedNCT01902940
Natural History in CCFDN and IBM Syndromes
Retrospective Cohort Study Assessing the Natural Course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and Sporadic and Hereditary Inclusion Body Myopathies (IBM)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 350 (actual)
- Sponsor
- Ludwig-Maximilians - University of Munich · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
So far, only limited data is available regarding the natural course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and sporadic and hereditary inclusion body myopathies (IBM). Several criteria and outcome measures have led to contradicting results. The investigators want to retrospectively assess the natural course of the disease in CCFDN and IBM patients according to the data recorded during clinical routine visits.
Detailed description
We wanted to assess the natural course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and sporadic and hereditary inclusion body myopathies (IBM) over 10 years to gain new insights in both conditions.
Conditions
- Inclusion Body Myositis, Sporadic
- Inclusion Body Myopathy, Autosomal-recessive
- Inclusion Body Myopathy, Autosomal-dominant
- Congenital Cataracts, Facial Dysmorphism, And Neuropathy
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Natural History | Assessment of natural history in IBM and CCFDN |
Timeline
- Start date
- 2013-06-01
- Primary completion
- 2013-09-01
- Completion
- 2013-10-01
- First posted
- 2013-07-18
- Last updated
- 2015-09-01
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01902940. Inclusion in this directory is not an endorsement.