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NCT03562806 Clinical Trial

MRI 3D UTE Hyper-Cones & ZTE for PET/MR Lung Attenuation Correction & for Lung Diagnostic Imaging

Lung Diseases Clinical Trial

Official title:
MRI 3D UTE Hyper-Cones & ZTE for PET/MR Lung Attenuation Correction & for Lung Diagnostic Imaging

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT03562806
Other study ID # 2017-00899
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 23, 2018
Est. completion date March 9, 2021

Study information
Verified date May 2022
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

MRI 3D UTE Hyper-Cones & ZTE for PET/MR lung attenuation correction & for lung diagnostic imaging

Description:

The primary objective is to clinically test the feasibility of 3D UTE Hyper-Cones & ZTE in capturing lung density of patients with lung diseases at reasonable clinical imaging times compared to standard MR lung protocols (LAVA-Flex, PROPELLER). Secondly, we want to investigate if Hyper-Cones & ZTE can be used for lung imaging such as vessels and air-pathways, oncological patients, lung nodules and lung infiltration & parenchyma pathophysiology such as chronic obstructive pulmonary disease.

Recruitment information / eligibility
Status Terminated
Enrollment 9
Est. completion date March 9, 2021
Est. primary completion date March 9, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - informed consent and signature - clinical PET/CT planned and performed at Wagi site in Schlieren - male or female patients - from 18 to 80 years of age. Exclusion Criteria: - same exclusion criteria as for the clinical PET/CT exam (i.e. pregnant women). Additional exclusion criteria: - standard exclusion criteria for clinical MRI (evaluated by clinical standard determined by MRI questionnaire).

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• PET/MR image acquisition
Acquisition of PET and MR sequences on SIGNA PET/MR device.

Locations
Country Name City State
Switzerland University Hospital Zurich, Department of Nuclear Medicine Zurich

Sponsors (1)
Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Confirm that lung density map extraction is feasible through Hyper-Cones & ZTE scanning. Confirm that lung density map extraction is feasible through Hyper-Cones & ZTE scanning. 1 year
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