Long QT Syndrome-Population Genetics and Cardiac Studies (LQTS)
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ClinicalTrials.gov Identifier: NCT00005176 |
Recruitment Status
:
Completed
First Posted
: May 26, 2000
Last Update Posted
: October 22, 2015
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Condition or disease |
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Cardiovascular Diseases Heart Diseases Ventricular Arrhythmia Long QT Syndrome |

Study Type : | Observational |
Actual Enrollment : | 2125 participants |
Observational Model: | Family-Based |
Time Perspective: | Prospective |
Official Title: | Long QT Syndrome-Population Genetics and Cardiac Studies |
Study Start Date : | August 1985 |
Actual Primary Completion Date : | April 2013 |
Actual Study Completion Date : | April 2013 |

- None. This is an observational study. [ Time Frame: By study end ]
Biospecimen Retention: Samples With DNA

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Ages Eligible for Study: | up to 100 Years (Child, Adult, Senior) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00005176
United States, New York | |
University of Rochester | |
Rochester, New York, United States, 14642 |
Principal Investigator: | Arthur Moss | University of Rochester |
Publications:
Responsible Party: | Arthur J. Moss, Professor, University of Rochester |
ClinicalTrials.gov Identifier: | NCT00005176 History of Changes |
Other Study ID Numbers: |
1053 R01HL033843-16 ( U.S. NIH Grant/Contract ) |
First Posted: | May 26, 2000 Key Record Dates |
Last Update Posted: | October 22, 2015 |
Last Verified: | October 2015 |
Additional relevant MeSH terms:
Syndrome Cardiovascular Diseases Heart Diseases Long QT Syndrome Disease |
Pathologic Processes Arrhythmias, Cardiac Heart Defects, Congenital Cardiovascular Abnormalities Congenital Abnormalities |