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Pilot Study: Safety of a Customized MRI System for Neonatal Imaging

NCT01522339 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2014-09-25

Study results available
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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).

Conditions

  • Safety of a Customized NICU MRI System

Interventions

DEVICE

GE OPTIMA MR430s with HDX/GE Electronics

MRI scan(s) for no longer than 60 minutes

Sponsors & Collaborators

  • Children's Hospital Medical Center, Cincinnati

    lead OTHER

Principal Investigators

  • Charles L Dumoulin, Ph.D. · Children's Hospital Medical Center, Cincinnati

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2012-04-30
Completion
2012-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01522339 on ClinicalTrials.gov