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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: |
NCT00528203 |
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Date of registration:
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10/09/2007 |
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Primary sponsor: |
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Public title:
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Establishing a Repository of Blood and DNA Samples From People With Sickle Cell Disease (Comprehensive Sickle Cell Centers Collaborative Genotype-Phenotype Database and Sample Repository)
Gen/Phen |
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Scientific title:
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Comprehensive Sickle Cell Centers (CSCC) Collaborative Genotype-Phenotype Database and Sample Repository |
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Date of first enrolment:
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August 2007 |
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Target sample size:
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3640 |
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Recruitment status: |
Terminated |
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URL:
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http://clinicaltrials.gov/show/NCT00528203 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Carolyn Hoppe, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Children's Hospital & Research Center Oakland |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Participating in the C-Data project
Exclusion Criteria:
- Unable to undergo blood collection
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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Anemia, Sickle Cell
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Secondary ID(s)
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517
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HL070587-08
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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