Clinical Trial Readiness for the Dystroglycanopathies
The purpose of the study is to describe the early signs and symptoms of the dystroglycanopathies, and to gather information that will be required for future clinical trials.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Clinical Trial Readiness for the Dystroglycanopathies|
fibroblasts, whole blood
|Study Start Date:||April 2006|
|Estimated Study Completion Date:||March 2020|
|Estimated Primary Completion Date:||March 2015 (Final data collection date for primary outcome measure)|
Muscular dystrophies are a diverse group of inherited disorders characterized by progressive muscle weakness and wasting. The disorders are caused by mutations, or changes, in genes. Genes are tiny pieces of inherited material (DNA) that direct the body to make certain kinds of proteins.
In this study, researchers will examine the clinical presentation of muscular dystrophy caused by abnormal glycosylation of alpha-dystroglycan. Patients with dystroglycanopathies could have mutations in one of the following genes: FKRP, fukutin, POMT1, POMT2, POMGnT1 or LARGE. Symptoms range from congenital muscular dystrophy that can also involve the brain and eye, through an adult-onset limb girdle muscular dystrophy.
The study involves a clinical evaluation at the University of Iowa. The evaluation includes muscle strength and motor ability testing, lung function testing, quality of life and activity assessment, and a review of past medical history. Portions of this evaluation will be repeated on a yearly basis. Financial assistance is available for travel to Iowa City. Support is also available for genetic testing for people with a dystroglycanopathy diagnosis based on muscle or skin biopsy analysis.
Knowledge gained from this study will improve healthcare recommendations for people with dystroglycanopathies, and provide a baseline for further study, including potential treatment options.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00313677
|Contact: Carrie Stephan, R.N. M.A.||(319) 356-2673|
|United States, Iowa|
|University of Iowa, 200 Hawkins Drive||Recruiting|
|Iowa City, Iowa, United States, 52242|
|Contact: Carrie Stephan, R.N. M.A. 319-356-2673|
|Principal Investigator:||Katherine Mathews, M.D.,||University of Iowa|
|Study Director:||Kevin Campbell, Ph.D.,||Co-Investigator|
|Study Director:||Steven A. Moore, M.D. Ph.D.||Co-Investigator|