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Natural History in CCFDN and IBM Syndromes

NCT01902940 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2015-09-01

No results posted yet for this study

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.

Conditions

  • Inclusion Body Myositis, Sporadic
  • Inclusion Body Myopathy, Autosomal-recessive
  • Inclusion Body Myopathy, Autosomal-dominant
  • Congenital Cataracts, Facial Dysmorphism, And Neuropathy

Interventions

OTHER

Natural History

Assessment of natural history in IBM and CCFDN

Sponsors & Collaborators

  • Ludwig-Maximilians - University of Munich

    lead OTHER

Principal Investigators

  • Maggie C Walter, MD, MA · Friedrich-Baur-Institute, Dept. of Neurology

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2013-09-30
Completion
2013-10-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01902940 on ClinicalTrials.gov