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NCT02644850 Clinical Trial

Comparison of Gated Blood-pool SPECT and Echocardiogram for Ventricular Function

Ventricular Dysfunction Clinical Trial

Official title:
Comparison of Gated Blood-pool SPECT Using CZT Camera and Echocardiogram for Ventricular Ejection Fraction Estimation

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02644850
Other study ID # 201508081RINA
Secondary ID
Status Recruiting
Phase N/A
First received December 29, 2015
Last updated December 30, 2015
Start date October 2015
Est. completion date December 2018

Study information
Verified date December 2015
Source National Taiwan University Hospital
Contact Mei-Fang Cheng, M.D.
Phone 886-2-23123456
Email meifang@ntuh.gov.tw
Is FDA regulated No
Health authority Taiwan: Ministry of Health and Welfare
Study type Observational [Patient Registry]

Clinical Trial Summary

To compare the calculated biventricular ejection fraction from cadmium-zinc-telluride (CZT) single photon emission computed tomography (SPECT) with planar equilibrium radionuclide angiography (ERNA), first-pass radionuclide ventriculography (FP-RNV) and echocardiogram.

Description:

To evaluate the feasibility of using CZT SPECT as an "all-in-one" technique to provide information on both left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) derived from a single examination and compare with the values from traditional planar ERNA, FP-RNV and echocardiography.

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date December 2018
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria:

- Patients underwent transthoracic echocardiogram and resting cardiac function within interval of 90 days of each other

Exclusion Criteria:

- Pregnancy

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan National Taiwan University Hospital and National Taiwan University College of Medicine Taipei

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measure the biventricular ejection fraction Through study completion, an average of 3 years No
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