University of California, Irvine
Irvine, California, 92697-1385, United States
Location status: Recruiting
Location contact
Virginia Kimonis, MD
CONTACT
Virginia Kimonis, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT01353430
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Irvine, California, 92697-1385, United States
Location status: Recruiting
Virginia Kimonis, MD
CONTACT
Virginia Kimonis, MD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Muscle disorders considered include:
AND
Eligible participants must also be:
Exclusion criteria
Individuals who report a different unrelated diagnosis will be excluded from the study. Testing to confirm different diagnoses will not be performed, instead patient will be questioned for this information and records will be obtained for confirmation of appropriate testing.
Those who are unable to provide consent for themselves will be excluded from participating in the study.
Contact information is provided by the study sponsor or research team.
University of California, Irvine
Other
Characterization of Familial Myopathy and Paget Disease of Bone
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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