Refinement and Assessment of New Magnetic Resonance Imaging (MRI) Technologies for Vascular, Abdominal, and Pelvic Exams
1 other identifier
interventional
20
1 country
1
Brief Summary
This study is being done to assess new Magnetic Resonance Imaging (MRI) technologies designed to improve MRI examinations of the vascular structures, abdomen, and pelvis regions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started May 2011
Longer than P75 for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 19, 2008
CompletedFirst Posted
Study publicly available on registry
August 20, 2008
CompletedStudy Start
First participant enrolled
May 2, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 14, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
January 14, 2020
CompletedJanuary 13, 2021
January 1, 2021
8.7 years
August 19, 2008
January 11, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Evaluation of new software in MRI vascular imaging
New software technology will be utilized to enhance MRI imaging of the vascular regions of the body.
1 year
Study Arms (1)
New MRI techniques
EXPERIMENTALNew hardware or software technologies designed to improve MRI (Magnetic Resonance Imaging) exams.
Interventions
MRI
Eligibility Criteria
You may qualify if:
- male or non-pregnant female patient
- years or older
- any ethnic background
- presenting to MRI for a clinically-ordered chest MRI exam.
You may not qualify if:
- Patients, who have electrically, magnetically or mechanically activated implants such as heart pacemaker, magnetic surgical clips, prostheses or implanted neurological stimulator.
- Pregnant patients or patients who are lactating.
- A patient who is claustrophobic
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Michiganlead
- General Electriccollaborator
- Philips Healthcarecollaborator
Study Sites (1)
University of Michigan Health Center
Ann Arbor, Michigan, 48109, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
William Masch, MD
University of Michigan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 19, 2008
First Posted
August 20, 2008
Study Start
May 2, 2011
Primary Completion
January 14, 2020
Study Completion
January 14, 2020
Last Updated
January 13, 2021
Record last verified: 2021-01
Data Sharing
- IPD Sharing
- Will not share