CompletedNot Applicable

Natural History in CCFDN and IBM Syndromes

Germany350 participantsStarted 2013-06

Plain-language 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.

Who can participate

SexALL

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Inclusion Criteria: * Clinical and/or genetic diagnosis of Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and sporadic and hereditary inclusion body myopathies (IBM) Exclusion Criteria: * Additional neuromuscular diseases

What they're measuring

Manual Muscle Strength assessed by Medical Research Council (MRC)

Timeframe: 6-months intervals

Trial details

NCT IDNCT01902940

SponsorLudwig-Maximilians - University of Munich

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2013-09

View on ClinicalTrials.gov More Inclusion Body Myositis, Sporadic trials