Overview

The Synergistic Effect of Dexmedetomidine on Propofol for Sedation for Pediatric Endoscopy

Status:
Active, not recruiting
Trial end date:
2022-07-12
Target enrollment:
0
Participant gender:
All
Summary
The primary aim of this study is to compare the propofol requirements of children who receive propofol with that of children who receive dexmedetomidine prior to propofol, for sedation for upper and lower endoscopic procedures.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Keira Mason
Treatments:
Dexmedetomidine
Propofol
Criteria
Inclusion Criteria:

- Ages 7-18 years who are scheduled for upper or lower endoscopic procedures at Boston
Children's Hospital and meets criteria to receive dexmedetomidine or propofol sedation
for upper and lower endoscopic procedures

- Provides written consent to participate in the research study

- For females of childbearing age, pregnancy test is negative

Exclusion Criteria:

- Do not meet established sedation criteria

- Refuses administration of study medication prior to sedation

- History of allergy, intolerance, or reaction to dexmedetomidine or propofol or
hypersensitivity

- Current, repaired or risk of Moya-Moya disease

- Recent stroke (cerebrovascular accident) within past 6 months

- Uncontrolled hypertension

- Concomitant use of opioids, beta antagonist, alpha 2 agonist or calcium channel
blocker

- Egg, soy or lecithin allergy

- BMI greater than 30 or weight above 110th percentile

- Refuses insertion of intravenous catheter while awake

- Currently receiving pharmacologic agents for hypertension or cardiac disease

- Currently receiving or has received digoxin within the past 3 months

- Active, uncontrolled gastroesophageal reflux - an aspiration risk

- Current (or within past 3 months) history of apnea requiring an apnea monitor

- Unstable cardiac status (life threatening arrhythmias, abnormal cardiac anatomy,
significant cardiac dysfunction)

- Craniofacial anomaly, which could make it difficult to effectively establish a mask
airway for positive pressure ventilation if needed

- Active, current respiratory issues that are different from the baseline status
(pneumonia, exacerbation of asthma, bronchiolitis, respiratory syncytial virus)