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OpenTrials
Completed

NCT Number: NCT03200132

Respiratory Motion Correction of Cardiac Combined Positron Emission Tomography and Magnetic Resonance Imaging (PET/MRI)

This study evaluates the possibility of Magnetic Resonance Imaging (MRI) based respiratory motion correction of simultaneously acquired cardiac Positron Emission Tomography (PET) images.

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Maastricht University Hospital

Maastricht, Limburg, 6229HX, Netherlands

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18F-FDG injection for clinical diagnostic PET/MRI or PET/CT

Exclusion criteria

  • Diet-suppressed myocardial uptake of 18F-FDG
  • General exclusion criteria for MRI (i.e. metallic implants, claustrophobia, pregnancy, etc.)
  • Not willing to be informed about incidental findings

Treatment and study plan

Cardiac PET/MRI

Diagnostic Test

For patients undergoing 18-Fluor- fluorodeoxyglucose (18F-FDG) PET/MRI or PET/Computed Tomography (CT), additional cardiac PET/MRI scans are acquired.

Primary outcomes

  1. Target-to-background ratio (TBR)

    Time frame: 15-20 minutes

Secondary outcomes

  1. Signal-to-noise ratio (SNR)

    Time frame: 15-20 minutes

Sponsors and collaborators

Lead sponsor

Maastricht University Medical Center

Other

Registry information

Important dates

Study start
2017
Primary completion
2021
Study completion
2021
First posted
Jun 27, 2017
Registry last updated
Apr 8, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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