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NCT00001881 · ClinicalTrials.gov registry record
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease
A clinical trial of Cardiomyopathy, Hypertrophic, Familial, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
- Completed
- Registry status
- 1
- Study location
NCT00001881: Completed study of Cardiomyopathy, Hypertrophic, Familial, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
NCT00001881 is a study of Cardiomyopathy, Hypertrophic, Familial that has completed, run by National Heart, Lung, and Blood Institute (NHLBI). The registry lists this as an open-ended (no fixed target) study. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00001881, a study of Cardiomyopathy, Hypertrophic, Familial, has completed, sponsored by National Heart, Lung, and Blood Institute (NHLBI).
- COMPLETED
- Registry status
- open-ended (no fixed target)
- Enrollment target
- 1
- Study location
Study Summary
Genetically inherited heart diseases (familial cardiomyopathies) are conditions affecting the heart passed on to family members through abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. In this study researchers hope to determine the signs and symptoms (clinical correlation) associated with specific genetic abnormalities causing inherited heart diseases. In order to do this, researchers plan to evaluate patients and family members of patients diagnosed with inherited heart disease. Patients participating in the study will undergo several tests including blood tests, electrocardiograms (EKG), and echocardiograms. Patients may also be asked to undergo an MRI of the heart to provide a clearer picture of it. Patients participating in this study may not be directly benefited by it. However, information gathered from the study may contribute to the medical care, treatment, and prevention of problems for others in the future.
Conditions Studied
Study Locations (1)
Maryland
- National Heart, Lung and Blood Institute (NHLBI) - Bethesda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | open-ended (no fixed target) |
| Start Date | 1999-03 |
| Est. Completion | 2001-04 |
What the finished NCT00001881 record still lists
NCT00001881 is an observational study that tracks outcomes without assigning an intervention. The registry lists this as an open-ended (no fixed target) study, common for long-running registries that collect data indefinitely.
The record links to 1 condition, with Cardiomyopathy, Hypertrophic, Familial appearing as the primary indexed condition, and to 0 interventions.
NCT00001881 reports a single indexed study location in Maryland.
Frequently Asked Questions
What is clinical trial NCT00001881 about?
NCT00001881 is a clinical study titled "Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease". Genetically inherited heart diseases (familial cardiomyopathies) are conditions affecting the heart passed on to family members through abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. In this study researchers hope to determine the...
What is the current status of trial NCT00001881?
This trial is currently completed. The enrollment target is open-ended (no fixed target). The study started on 1999-03. Estimated completion is 2001-04.
What conditions does trial NCT00001881 study?
This clinical trial studies the following conditions: Cardiomyopathy, Hypertrophic, Familial.
Who is sponsoring clinical trial NCT00001881?
This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 501 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00001881 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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