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Clinical Trial Summary

The investigators are researching families with inherited inclusion body myopathy (IBM) and/or Paget disease of bone (PDB) and/or dementia (FTD) which is also called IBMPFD. IBMPFD is caused by mutations in the VCP gene. Our main goal is to understand how changes in the VCP gene cause the muscle, bone and cognitive problems associated with the disease. The investigators are collecting biological specimen such as blood and urine samples, family and medical histories, questionnaire data of patients with a personal or family history of VCP associated disease. Participants do not need to have all symptoms listed above in order to qualify. A select group of participants may be invited to travel to University of California, Irvine for a two day program of local procedures such as an MRI and bone scan. Samples are coded to maintain confidentiality. Travel is not necessary except for families invited for additional testing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01353430
Study type Observational
Source University of California, Irvine
Contact Virginia Kimonis, MD
Phone 949 824 0571
Email vkimonis@uci.edu
Status Recruiting
Phase
Start date November 15, 2007
Completion date December 2026

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