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Dynamic CT Myocardial Perfusion Imaging

Diagnostic Value and Practicability of Dynamic CT Stress and Rest Myocardial Perfusion Imaging in Daily Clinical Practice - A Monocentric Prospective Diagnostic Study

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02593838
Enrollment
43
Registered
2015-11-02
Start date
2015-09-30
Completion date
2021-09-28
Last updated
2021-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Brief summary

This study aims at evaluating the feasibility of CT myocardial perfusion imaging in daily clinical practice and compare it to SPECT perfusion imaging in order to assess sensitivity and specifity of CT myocardial perfusion imaging compared to SPECT.

Detailed description

If after the clinically indicated CCTA a myocardial perfusion examination is indicated, first a single ultra low dose CT scan will be performed to look for late enhancement of potentially scarred myocardium. Together with the contrast agent co-injection of the clinically indicated tracer 99mTc-Tetrofosmin will be performed for later scintigraphic perfusion evaluation. After stress perfusion imaging CT rest perfusion imaging will be performed in a similar fashion. After acquisition of CT rest perfusion images scintigraphic stress and rest image acquisition will be performed as in daily clinical routine with an additional administration of 99mTc-Tetrofosmin resting dose if necessary. CT stress and rest perfusion will be compared to the clinically indicated and well established SPECT examination.

Interventions

OTHERCT-MPI and SPECT-MPI

All patients undergo CT-MPI plus SPECT-MPI

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Referral for cardiac hybrid imaging with CCTA and SPECT * Male and Female subjects 18 years of age or older, * Written informed consent by the participant after information about the project

Exclusion criteria

* Contraindications for CCTA (including renal failure with a GFR \<60ml/min/1.73m2, allergies to ionidated constrast agents) * Inability to follow the examination procedure due to language barriers, mental disease, dementia etc. * Pregnancy or breast feeding * Known allergies to iodinated contrast agent (Visipaque ®), 99mTc-Tetrofosmin (Myoview ®), betablockers (Beloc i.v. ®) or nitrates (Isoket -Spray®) * Hypersensitivity to adenosine * Asthma bronchiale

Design outcomes

Primary

MeasureTime frameDescription
Validation of CT-MPI against SPECT-MPI2 yearsSensitivity and specificity of CT-MPI to diagnose obstructive coronary artery disease using SPECTR-MPI as the standard reference

Secondary

MeasureTime frameDescription
Parameters influencing image quality of CT-MPI - Body physique2 yearsCorrelation between visually assessed image quality of CT-MPI and patient's body mass index
Parameters influencing image quality of CT-MPI - Heart rate2 yearsCorrelation between visually assessed image quality of CT-MPI and patient's heart rate during the scan

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026