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NCT00027196 · ClinicalTrials.gov registry record
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease
A clinical trial, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
- Completed
- Registry status
- 9,999,999
- Enrollment target
NCT00027196: Completed study, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
NCT00027196 is a clinical trial that has completed, run by National Heart, Lung, and Blood Institute (NHLBI). The registered enrollment target is 9,999,999 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00027196 has completed, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
- COMPLETED
- Registry status
- 9,999,999 participants
- Enrollment target
Study Summary
Genetically inherited heart diseases (familial cardiopathies) are conditions affecting the heart passed on to family members by abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. Researchers are interested in learning more about the specific genetic abnormalities causing heart diseases. In addition, they would like to find out how these abnormal genes can contribute to the development of other medical problems. In order to do this, researchers plan to study patients and family members of patients diagnosed with genetically inherited heart disease. Those people participating in the study will undergo a variety of tests including blood tests, echocardiograms, and magnetic resonance imaging studies (MRI). These tests will be used to help researchers find the genetic problem causing the familial cardiopathy. Researchers hope that the information gathered from this study can be used to develop better medical care through early diagnosis, management, and treatment plans.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9,999,999 participants |
| Start Date | 1998-04 |
| Est. Completion | 2003-04 |
What the finished NCT00027196 record still lists
NCT00027196 is an observational study that tracks outcomes without assigning an intervention. Its 9,999,999 participants enrollment target places it among the larger protocols in the corpus.
The record links to 0 conditions, and to 0 interventions.
NCT00027196 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00027196 about?
NCT00027196 is a clinical study titled "Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease". Genetically inherited heart diseases (familial cardiopathies) are conditions affecting the heart passed on to family members by abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. Researchers are interested in learning more about the s...
What is the current status of trial NCT00027196?
This trial is currently completed. The enrollment target is 9,999,999 participants. The study started on 1998-04. Estimated completion is 2003-04.
Who is sponsoring clinical trial NCT00027196?
This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 501 total clinical trials registered on ClinicalTrials.gov.
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