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Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
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Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
ClinicalTrials.gov Identifier: | NCT00005176 |
To investigate the clinical, genetic and cardiologic aspects of the Long QT Syndrome, a predominantly hereditary disease with episodic malignant arrhythmias and sudden death, and a demonstrated gene linkage in a large pedigree.
Study Type: | Observational |
Study Start Date: | August 1985 |
Study Completion Date: | June 2008 |
Primary Completion Date: | June 2008 (Final data collection date for primary outcome measure) |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
No eligibility criteria
Study ID Numbers: | 1053 |
Study First Received: | May 25, 2000 |
Last Updated: | July 23, 2008 |
ClinicalTrials.gov Identifier: | NCT00005176 History of Changes |
Health Authority: | United States: Federal Government |
Heart Diseases Cardiovascular Abnormalities Long QT Syndrome |
Congenital Abnormalities Heart Defects, Congenital Arrhythmias, Cardiac |
Disease Pathologic Processes Heart Diseases Cardiovascular Abnormalities Syndrome |
Long QT Syndrome Cardiovascular Diseases Congenital Abnormalities Heart Defects, Congenital Arrhythmias, Cardiac |