Dexmedetomidine and Propofol in Children With History of Obstructive Sleep Apnea
Effect of Increasing Depth of Dexmedetomidine and Propofol Anesthesia on Upper Airway Morphology in Children With History of Obstructive Sleep Apnea
1 other identifier
interventional
60
1 country
1
Brief Summary
The purpose of this research study is to examine the effects of two commonly used anesthetic drugs, dexmedetomidine and propofol, have on the shape and muscle tone of the upper airway in children, adolescents, and young adults with a history of obstructive sleep apnea (OSA) having an MRI scan. The results of this study will help in making the best decisions regarding the anesthesia medications that are most appropriate for children, adolescents, and young adults with OSA during MRI studies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4
Started Jun 2009
Typical duration for phase_4
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
Study Start
First participant enrolled
June 1, 2009
CompletedFirst Submitted
Initial submission to the registry
April 21, 2011
CompletedFirst Posted
Study publicly available on registry
April 29, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2011
CompletedResults Posted
Study results publicly available
February 23, 2016
CompletedAugust 8, 2018
August 1, 2018
2.4 years
April 21, 2011
August 20, 2015
August 6, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Cross Sectional Area of the Pharyngeal Airway
The primary outcome measures will be the cross sectional area of the pharyngeal airway of the patients measured at two levels soft palate (nasopharyngeal) and base of the tongue (retroglossal). Magnetic resonance images of the airway were obtained during low (1 mcg/kg/hr) and high (3 mcg/kg/hr) doses of DEX or low (100 mcg/kg/m) and high (200 mcg/kg/m) doses of Propofol. All were administered through an intravenous (IV) catheter.
during MRI within first 10 minutes of scanning
Secondary Outcomes (4)
Obstructive Index Until Recovery Room Discharge
During MRI and until recovery room discharge - approximately 30-250 minutes
Respiratory Disturbance Index
During MRI and until recovery room discharge - approximately 30-250 minutes
Needed Artificial Airway
During MRI and until recovery room discharge - approximately 30-250 minutes
Room Air SpO2
During MRI and until recovery room discharge - approximately 30-250 minutes
Study Arms (2)
Propofol
ACTIVE COMPARATORDexmedetomidine
ACTIVE COMPARATORInterventions
Once an IV is in place, atropine 10 mcg/kg will be given. Loading dose of dexmedetomidine 1 mcg/kg will be administered over 10 minutes followed by a continuous infusion of dexmedetomidine at rate of 1 mcg/kg/h using a syringe pump.
Once an IV is in place, atropine 10 mcg/kg will be given. Loading dose of propofol 2 mg/kg will be administered over 2 minutes followed by a continuous infusion of propofol at rate of 100 mcg/kg/minute using a syringe pump.
Eligibility Criteria
You may qualify if:
- Patients with documented history of OSA by polysomnography who require anesthesia for MRI sleep study or MRI brain imaging study.
- Subjects must be 12 months to 25 years of age (inclusive)
- Either the subject (if subject's age is 18-25) or the subject's legally authorized representative has given written informed consent to participate in the study
You may not qualify if:
- 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).
- The subject is allergic to or has a contraindication to propofol or dexmedetomidine.
- The subject has a tracheostomy or other mechanical airway device
- The subject is not scheduled to receive anesthesia-sedation care for the MRI
- The subject has a history or a family (parent or sibling) history of malignant hyperthermia.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
Related Publications (33)
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PMID: 15208134BACKGROUNDIbacache ME, Munoz HR, Brandes V, Morales AL. Single-dose dexmedetomidine reduces agitation after sevoflurane anesthesia in children. Anesth Analg. 2004 Jan;98(1):60-63. doi: 10.1213/01.ANE.0000094947.20838.8E.
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PMID: 18811855BACKGROUNDEastwood PR, Platt PR, Shepherd K, Maddison K, Hillman DR. Collapsibility of the upper airway at different concentrations of propofol anesthesia. Anesthesiology. 2005 Sep;103(3):470-7. doi: 10.1097/00000542-200509000-00007.
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PMID: 10702460BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Limitations and Caveats
Failure to standardize mouth opening, due to stimulation of the subject during manipulation of the mouth No baseline measurements were obtained while awake Many patients had Downs syndrome so the results may not apply across all patients with OSA
Results Point of Contact
- Title
- Dr. Mohamed Mahmoud
- Organization
- Cincinnati Children's Hosptial Medical Center
Study Officials
- PRINCIPAL INVESTIGATOR
Mohamed Mahmoud, MD
Children's Hospital Medical Center, Cincinnati
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 21, 2011
First Posted
April 29, 2011
Study Start
June 1, 2009
Primary Completion
November 1, 2011
Study Completion
November 1, 2011
Last Updated
August 8, 2018
Results First Posted
February 23, 2016
Record last verified: 2018-08