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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00661752
Other study ID # quarter-time cardiac SPECT
Secondary ID
Status Completed
Phase N/A
First received April 8, 2008
Last updated August 25, 2008
Start date May 2007
Est. completion date January 2008

Study information

Verified date August 2008
Source St. Luke's-Roosevelt Hospital Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

A new, innovative software image processing method, wide beam reconstruction (WBR), utilizes resolution recovery and incorporates Poisson noise-reduction into the reconstruction process of NM images. This method facilitates the reconstruction of low count density myocardial perfusion SPECT images. Preliminary research indicates that SPECT acquisition time consequently can be reduced by 60% (less than 5 minutes) for rest and by 75% (just over 3 minutes) for stress, while tomographic image quality is maintained, or even improved. Such a decrease in image acquisition time decreases patient discomfort during the tomographic acquisition, decreases the opportunity for patient motion, and improves laboratory efficiency.


Description:

Standard full-time SPECT will be processed using FBP and compared to 3-minute stress and 5-minute rest scans processed with WBR. The following scan parameters will be evaluated: image quality; perfusion defect extent, severity, and reversibility; transient ischemic dilatation; left ventricular end-diastolic volume; left ventricular end-systolic volume; left ventricular ejection fraction; and regional wall motion and wall thickening abnormalities. These parameters will be assessed visually by experienced Nuclear physicians (at least 2 blinded readers) and quantitatively using several different commercially available software programs.


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date January 2008
Est. primary completion date August 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient is clinically stable

- Patient is able to tolerate additional 8 minutes of scanning

- Patient is willing to undergo additional 8 minutes of scanning

Exclusion Criteria:

- Unstable patient

- Non-consenting patient

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Device:
quarter-time stress scans reconstructed by WBR (4SPS) - Xpress3.Cardiac
Comparison of the diagnostic quality of quarter-time WBR stress with stress studies generated via FBP and half-time WBR
quarter-time rest scans reconstructed by WBR (6/8/10 SPS) - Xpress3.Cardiac
Comparison of the diagnostic quality of 6 SPS quarter-time rest acquisitions with FBP and half-time WBR rest studies; simulated 8 SPS and 10 SPS quarter-time rest acquisitions are also compared to FBP and half-time WBR rest studies.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
St. Luke's-Roosevelt Hospital Center

Outcome

Type Measure Description Time frame Safety issue
Primary Image quality of quarter-time WBR images is equivalent/superior to full-time FBP March 2008 No
Secondary Image quality of quarter-time WBR is equivalent/superior to half-time WBR March 2008 No
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