A Pilot Study to Assess the Amnesic Properties of Dexmedetomidine in Pediatric Patients
Completed
Conditions studied: Memory, Dexmedetomidine
In brief
The goal of this study is to determine the effects of dexmedetomidine on memory and recall of children who are receiving dexmedetomidine sedation administered for magnetic resonance imaging (MRI) studies. Dexmedetomidine is currently the standard drug for sedation for diagnostic (MRI, computerized tomography (CT) and Nuclear Medicine) radiological studies at Boston Children's Hospital (BCH). The effect of dexmedetomidine on memory and recall in children has not been studied.
Key facts
- Study ID
- NCT02354378
- Run by
- Boston Children's Hospital
- People needed
- 84
- Starts
- 2012-08-01
- Expected to finish
- 2015-03-01
- Last updated by the study team
- 2019-02-28
Who can join
Age: 4 and older, up to 14. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The patient must be between 4 and 14 yrs of age and be undergoing a therapeutic or diagnostic procedure with or without sedation
- The patient must be able to comprehend and perform the task (naming pictures)
- The patient must have a minimum weight of 8 kg
You may not qualify if…
- Allergy to Dexmedetomidine (for those patients requiring sedation)
- Procedure of short duration (< 15 min)
- Pregnancy
- Recent use (within 5 half-lives) of centrally acting medications that could affect concentration (e.g. diphenhydramine)
Where it is running
- Boston Children's Hospital — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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