Breath-hold Cardiac Hybrid SPECT/CCTA

NCT ID: NCT02469051

Last Updated: 2016-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-05-31

Study Completion Date

2016-05-31

Brief Summary

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This study aims at combining inspiration breath-hold myocardial perfusion SPECT with coronary CT angiography.

Detailed Description

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Conditions

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Coronary Artery Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Breathhold SPECT-MPI vs. standard freebreathing SPECT-MPI

Group Type OTHER

Breathhold SPECT-MPI

Intervention Type DEVICE

Respiratory triggered SPECT myocardial perfusion imaging

Standard freebreathing SPECT-MPI

Intervention Type DEVICE

Clinically indicated, standard non-respiratory triggered SPECT myocardial perfusion imaging

Coronary CT angiography

Intervention Type DEVICE

Clinically indicated coronary CT angiography serving as standard of reference

Interventions

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Breathhold SPECT-MPI

Respiratory triggered SPECT myocardial perfusion imaging

Intervention Type DEVICE

Standard freebreathing SPECT-MPI

Clinically indicated, standard non-respiratory triggered SPECT myocardial perfusion imaging

Intervention Type DEVICE

Coronary CT angiography

Clinically indicated coronary CT angiography serving as standard of reference

Intervention Type DEVICE

Other Intervention Names

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CCTA

Eligibility Criteria

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Inclusion Criteria

* Referral for cardiac hybrid SPECT/CCTA
* 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 coronary CT angiography (including renal failure with a GFR \<30ml/min/1.73m2, allergies to iodinated contrast agents)
* Pregnancy or breast-feeding
* Previous coronary revascularisation
* Inability to follow the examination procedure (e.g. due to language barriers, severe mental disease etc
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Department of Nuclear Medicine, University Hospital Zurich

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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USZ-2015-0098

Identifier Type: -

Identifier Source: org_study_id

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