Study Stopped
Tested MR sequence was inferior in preliminary evaluation
MRI 3D UTE Hyper-Cones & ZTE for PET/MR Lung Attenuation Correction & for Lung Diagnostic Imaging
1 other identifier
interventional
9
1 country
1
Brief Summary
MRI 3D UTE Hyper-Cones \& ZTE for PET/MR lung attenuation correction \& for lung diagnostic imaging
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2018
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 23, 2018
CompletedStudy Start
First participant enrolled
May 23, 2018
CompletedFirst Posted
Study publicly available on registry
June 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 9, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 9, 2021
CompletedMay 23, 2022
May 1, 2022
2.8 years
May 23, 2018
May 16, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
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
Study Arms (1)
PET/MR (single arm)
EXPERIMENTALPET and MR sequence acquisition on SIGNA PET/MR device
Interventions
Acquisition of PET and MR sequences on SIGNA PET/MR device.
Eligibility Criteria
You may qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Zurich, Department of Nuclear Medicine
Zurich, 8091, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Martin Huellner, M.D.
University Hospital, Zürich
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 23, 2018
First Posted
June 20, 2018
Study Start
May 23, 2018
Primary Completion
March 9, 2021
Study Completion
March 9, 2021
Last Updated
May 23, 2022
Record last verified: 2022-05
Data Sharing
- IPD Sharing
- Will not share