NCT00639704

Brief Summary

The purpose of this study is to compare the MRI results with the new SPECT image reconstruction method, this study will allow us to determine whether a new more accurate method of looking at the heart by nuclear study can be used in routine clinical use.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
6

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 1996

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 1996

Completed
12.2 years until next milestone

First Submitted

Initial submission to the registry

March 12, 2008

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 20, 2008

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2011

Completed
Last Updated

December 14, 2023

Status Verified

December 1, 2023

Enrollment Period

15.6 years

First QC Date

March 12, 2008

Last Update Submit

December 13, 2023

Conditions

Cardiac

Keywords

MRISPECTCardiac function

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Subjects who are being evaluated for cardiac function/perfusion

You may qualify if:

  • subjects scheduled for cardiac SPECT
  • subjects 18 years old or older

You may not qualify if:

  • Females who are pregnant or think that they are pregnant will be excluded in this study.
  • Subjects who have a pacemaker, internal defibrillator, prostheses, artificial heart valves, cardiac stents, surgical clips, or TENS (transcutaneous electric nerve stimulator)
  • Subjects who are 300 lbs and over

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

SUNY Upstate Medical University

Syracuse, New York, 13210, United States

Location

Study Officials

  • Andrzej Krol, PhD

    State University of New York - Upstate Medical University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

March 12, 2008

First Posted

March 20, 2008

Study Start

January 1, 1996

Primary Completion

August 1, 2011

Study Completion

August 1, 2011

Last Updated

December 14, 2023

Record last verified: 2023-12

Locations

US(1)