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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00001871 |
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Date of registration:
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03/11/1999 |
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Primary sponsor: |
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Public title:
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Study of Muscle Abnormalities in Patients With Specific Genetic Mutations
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Scientific title:
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An Exploratory Study of Skeletal Muscle Abnormalities in Patients With Mutations in Alpha-Tropomyosin and PABP2 Genes |
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Date of first enrolment:
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January 1999 |
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Target sample size:
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80 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00001871 |
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Study type:
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Observational |
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Study design:
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N/A
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Countries of recruitment
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United States
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Key inclusion & exclusion criteria
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Patients will be of either gender, aged 10-80 years old, in whom alpha-tropomyosin and
PABP2 genotypes have been determined under protocols 87-H-0057 and 98-H-0100.
No bleeding diathesis.
Negative urine test for pregnancy.
No skin infection at site of biopsy.
Age minimum:
N/A
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Cardiomyopathy, Hypertrophic
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Muscular Dystrophy, Oculopharyngeal
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Secondary ID(s)
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99-H-0036
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990036
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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