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NCT00328315 Clinical Trial

Cardiac SPECT With Rotating Slant Hole Collimator

Chest Pain Clinical Trial

Official title:
Myocardial Perfusion SPECT Using a Rotating Multi-segment Slant-hole Collimator

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00328315
Other study ID # NO:05-06-03-02
Secondary ID R01 EB 0019-83
Status Completed
Phase
First received May 18, 2006
Last updated April 4, 2018
Start date October 2006
Est. completion date December 2007

Study information
Verified date April 2018
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal is to conduct a clinical pilot study to evaluate the use of a rotating multi-segment slant-hole collimator in the detection of myocardial defects.

Description:

Myocardial perfusion SPECT is recognized as an effective clinical diagnostic imaging technique in the assessment of myocardial perfusion and coronary artery diseases. It is the most important clinical application of SPECT imaging techniques.

The goal is to conduct a clinical pilot study to evaluate the use of rotating multi-segment slant-hole (RMSSH) SPECT in the detection of myocardial defects especially in very sick patients in the nuclear medicine clinics, emergence room, and intensive care units. Comparison of the clinical utilities of the cardiac RMSSH SPECT technique with conventional cardiac planar and SPECT with parallel-hole collimation will also allow us to evaluate the potential application of the technique to a wider patient population.

The objective of this study is to test the hypothesis that quantitative 99mTc myocardial perfusion RMSSH SPECT provides similar diagnostic accuracy in patients with cardiac diseases as conventional SPECT imaging techniques.

Recruitment information / eligibility
Status Completed
Enrollment 5
Est. completion date December 2007
Est. primary completion date December 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Males and Females 18-80 who are scheduled for a clinical Cardiac Stress Test

Exclusion Criteria:

- Pregnant Women and Children

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Johns Hopkins Outpatient Center Baltimore Maryland

Sponsors (2)
Lead Sponsor Collaborator
Johns Hopkins University National Institute for Biomedical Imaging and Bioengineering (NIBIB)

Country where clinical trial is conducted

United States, 

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