Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05303987

Dexmedetomidine Versus Propofol Sedation for Drug-Induced Sleep Endoscopy in Pediatric Obstructive Sleep Apnea

Trial of Dexmedetomidine Versus Propofol Sedation for Drug-Induced Sleep Endoscopy in Pediatric Obstructive Sleep Apnea

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Erin Kirkham · Academic / Other
Sex
All
Age
3 Years – 11 Years
Healthy volunteers
Not accepted

Summary

This research study is designed to learn, first, whether two anesthetics have different effects on collapse seen within the upper airway during sleep endoscopy. A second purpose is to learn whether collapse at several levels of the upper airway is associated with obstructive sleep apnea that persists after adenotonsillectomy, the surgery that removes the tonsils and adenoids.

Conditions

Interventions

TypeNameDescription
DRUGPropofol sedationAfter induction with sevoflurane then Propofol will be initiated. If adequate sedation cannot be attained then a ketamine rescue can be given.
DRUGDexmedetomidine sedationAfter induction with sevoflurane then Dexmedetomidine will be given. If adequate sedation cannot be attained then a ketamine rescue can be given.

Timeline

Start date
2022-10-05
Primary completion
2026-08-31
Completion
2026-08-31
First posted
2022-03-31
Last updated
2026-01-29

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05303987. Inclusion in this directory is not an endorsement.