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Two Anesthetic Techniques in Magnetic Resonance Imaging (MRI)

NCT00894751 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 98

Last updated 2020-09-21

No results posted yet for this study

Summary

The goal of this study is to determine if there is a significant difference in the quality of care between the investigators' two standard anesthesia techniques for children undergoing a MRI of the body and/or extremity MRI. Quality of care will be measured by time spent in the MRI room as well as parental satisfaction, frequency of interruptions of the MRI scan, incidence-severity of respiratory complications, post anesthesia agitation, and time spent in the induction room, MRI room, and Post-Anesthesia Care Unit (PACU).

Conditions

  • Magnetic Resonance Imaging
  • Anesthesia

Interventions

DRUG

dexmedetomidine

dexmedetomidine general anesthesia for MRI

DRUG

propofol

propofol general anesthesia for MRI

Sponsors & Collaborators

  • Children's Hospital Medical Center, Cincinnati

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Months
Max Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2011-01-31
Completion
2011-12-31

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 NCT00894751 on ClinicalTrials.gov