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Cardiovascular Disease Screening

Suburban/NHLBI Cardiovascular Disease Screening Protocol

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00483951
Enrollment
1325
Registered
2007-06-08
Start date
2008-01-28
Completion date
2020-11-03
Last updated
2021-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acquired Heart Disease, Atherosclerosis, Congenital Heart Disease, Myocardial Infarction, Myocardial Ischemia

Keywords

Transthoracic echocardiography, Ischemia, Cardiovascular Disease

Brief summary

This study will evaluate volunteers 18 years of age and older to see if they qualify for one of NHLBI s research studies. Tests include the following: * General medical evaluation, which may include blood tests, chest x-ray, electrocardiogram (ECG) and echocardiogram (heart ultrasound). * Other tests as appropriate, such as magnetic resonance imaging (MRI), cardiac computed tomography (CT scan of the heart), nuclear stress test and echocardiography stress test. * X-ray contrast studies of the heart and blood vessels. (These may be excluded in patients with kidney risk factors.)

Detailed description

This is a screening protocol. This protocol allows two functions: 1) the protocol allows physicians in the Suburban/NHLBI Cardiovascular Imaging program to evaluate patients referred to the program with clinically indicated studies and research studies. 2) It is also designed to determine if patients may be suitable candidates for one of our NHLBI research protocols. Patients greater than or equal to 18 years of age referred for possible cardiovascular disease will be enrolled in the protocol for a period of one year. At one year, patients will either be: 1) transferred to one of our specific research MRI or CT protocols, 2) removed from the screening protocol and made inactive, or 3) re-enrolled on the screening protocol with the patient s consent.

Interventions

DEVICEToshiba Aquilion ONE CT

The Toshiba Aquilion ONE CT system has the ability to acquire whole organ volume images in a single rotation by utilizing an x-ray detector that is configured as 320 detector rows with a 0.5 mm width, providing a z-axis coverage of 16 cm of anatomy.

DEVICESWiemens MRI scanner

Investigational or research MRI coils may be used in the protocol. The coils are noninvasive devices external to the body. The coils act as antennae to receive small radiofrequency signals out of the body. Coils of the type we use are used daily in clinical MRI practice.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
Lead SponsorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ELIGIBILITY CRITERIA: No one will be excluded from this study based on race, gender, or ethnicity. A. General Inclusion Criteria: * Age greater than or equal to 18 * Capable of giving informed consent. B. General

Exclusion criteria

* Pregnant women (uncertain patients will have urine or blood testing). * Decompensated heart failure (unable to lie flat in bed). Test Specific

Design outcomes

Primary

MeasureTime frameDescription
Complete characterization of patients for screening purpose onto a research protocol.OngoingComplete characterization of patients for the purpose of deciding whether they are eligible for research protocols run by the Cardiovascular Branch.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026