Two Anesthetic Techniques in Magnetic Resonance Imaging (MRI)

Anesthesia Clinical Trial

Official title:

A Qualitative Comparison of Two Anesthetic Techniques in Children Undergoing Magnetic Resonance Imaging

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00894751
• Other study ID #: 2008-0281
• Status: Terminated
• Phase: Phase 1
• Start date: January 2009
• Est. completion date: December 2011

Study information

• Verified date: August 2020
• Source: Children's Hospital Medical Center, Cincinnati
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 98
• Est. completion date: December 2011
• Est. primary completion date: January 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 12 Months to 7 Years

Eligibility

Inclusion Criteria:

1. Subjects presenting as out-patients, scheduled to receive an anesthetic for MRI of body (spine, chest, abdomen, and/or pelvis) and/or extremity (arm and/or leg).

2. The subject must be a candidate for both anesthetic techniques. This decision will be made by a staff member of the Department of Anesthesiology. This staff member will not be a member of the study team and will obtain the consent for Anesthesia.

3. The subjects must be 12 months to 7 years (inclusive of the seventh year).

4. The subject's legally authorized representative has given written informed consent to participate in the study.

Exclusion Criteria:

1. The subject is residing in the Pediatric Intensive Care Unit, the Cardiac Intensive Care Unit, or Neonatal Intensive Care Unit.

2. Anxiolytic medication is ordered before the MRI (e.g., midazolam or ketamine).

3. The subject has a history or a family (parent or sibling) history of malignant hyperthermia.

4. The subject has life-threatening, medical conditions (American Society of Anesthesiologists Physical Status 4, 5 or 6).

• The American Society of Anesthesiologists (ASA) classification scale is a measure of physical status or how healthy the patient is.

• For our study, we will focus on children which are defined as ASA I, II or III which means a healthy child (ASA I), a child with a systemic disease that is mild and well controlled (ASA II) or a child with systemic disease that is severe and controlled (ASA III).

5. The subject is allergic to or has a contraindication to any of the drugs used in the study.

6. The subject has previously been treated under this protocol.

7. The subject has a tracheostomy or other mechanical airway device.

8. The subject has received within the past 12 hours an oral or intravenous alpha-adrenergic, beta-adrenergic agonist, or antagonist drugs (e.g., clonidine, propranolol, albuterol).

9. The subject is not scheduled to receive anesthesia-sedation care for the MRI.

10. The subject received one of the anesthetic regimens for the same MRI during the past six months.

Related Conditions & MeSH terms

• Anesthesia
• Magnetic Resonance Imaging

Intervention

Drug:
• dexmedetomidine
dexmedetomidine general anesthesia for MRI
• propofol
propofol general anesthesia for MRI

Locations

Country	Name	City	State
United States	Cincinnati Children's Medical Center	Cincinnati	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Children's Hospital Medical Center, Cincinnati

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary outcome variable will be the time spent in the MRI room		2 years
Secondary	Secondary outcome variables include incidence-severity of respiratory complications		2 years