At a glance
ClinicalIndex Comparison RecordN/ACompleted· 15 enrolled
Drug / intervention
GE OPTIMA MR430s with HDX/GE Electronicsdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Pilot Study: Safety of a Customized MRI System for Neonatal Imaging
Children's Hospital Medical Center, Cincinnati·interventional·Posted Jan 31, 2012·Updated Sep 25, 2014
In Brief
A clinical study evaluating GE OPTIMA MR430s with HDX/GE Electronics for Safety of a Customized NICU MRI System. Completed, enrolled 15 participants across 1 site.
Detailed Summary
The purpose of this study is to determine the safety of a customized MRI scanner and gather preliminary data on image quality in a group of 10 medically stable infants admitted to the Neonatal Intensive Care Unit (NICU) at Cincinnati Children's Hospital Medical Center (CCHMC).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSafety of a Customized NICU MRI System
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedJan 2012
Enrollment StartFeb 2012
Primary CompletionApr 2012
TodayJul 2026
First PostedJan 31, 2012
Enrollment StartFeb 1, 2012
Primary CompletionApr 1, 2012
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 14.4 years ago
Interventions
GE OPTIMA MR430s with HDX/GE Electronicsdevice
MRI scan(s) for no longer than 60 minutes