Reducing Radioisotope Dose: the Half-Dose CZT Study



Status:Recruiting
Conditions:Peripheral Vascular Disease, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - 90
Updated:2/10/2017
Start Date:January 2012
End Date:November 2017
Contact:Christopher Mattair
Email:cbmattair@houstonmethodist.og
Phone:713-363-9956

Use our guide to learn which trials are right for you!

Reducing Radioisotope Dose in Regadenoson SPECT Myocardial Perfusion Imaging: Comparison of Half-Dose Scans Using a Novel Solid-State-Detector Dedicated Cardiac Camera to Full Dose Scans Acquired On Standard Equipment

This is a pilot study to see whether cardiac imaging can be performed using half the
standard dose of radioisotope.

The aim of this study is to compare the image quality of the half radioisotope dose scans
obtained using a CZT (cadmium zinc telluride) camera with scans acquired using a standard of
care imaging protocol/radioisotope dose performed on a traditional (conventional) camera.

The proposed strategy of a half dose/extended time protocol with the CZT camera should yield
a similar count activity and consequently image quality equivalent to that detected by a
conventional SPECT system.

Inclusion Criteria:

- ≥ 18 years of age and referred for a clinically-indicated stress SPECT MPI study

- suspected or known coronary artery disease

- written informed consent

Exclusion Criteria:

- Evidence of a normal baseline scan after at least 50% of the protocol acquired
baseline scans have been interpreted as being normal

- Participation in another investigational study within the preceding month

- Pregnant and/or breast-feeding female

- ECG evidence of left bundle branch block or paced rhythm

- Evidence of non-ischemic cardiomyopathy

- Presence of hypertrophic cardiomyopathy and/or severe valvular heart disease

- Severe claustrophobia or inability to lie flat for 20 minutes (the anticipated amount
of time to complete the procedure)

- Known allergy to technetium-99m

- Potential contraindications to regadenoson use, due to severe lung disease; severe
bradycardia (heart rate < 40 beats/min); second- or third degree atrioventricular
heart block; sick sinus syndrome; long QT syndrome; severe hypotension; or
decompensated heart failure.
We found this trial at
1
site
6550 Fannin St
Houston, Texas 77030
(713) 790-3311
Principal Investigator: Su Min Chang, MD
Phone: 713-363-9956
Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
?
mi
from
Houston, TX
Click here to add this to my saved trials