Overview
Sevoflurane and Laryngeal Reflex Responses in Pediatric Patients
Status:
Terminated
Terminated
Trial end date:
2008-08-01
2008-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To describe laryngeal and respiratory reflex responses after controlled laryngeal stimulation in pediatric patients anesthetized with sevoflurane and to compare the evoked responses at two levels of anesthesia. To determine whether laryngeal and respiratory reflex responses after controlled laryngeal stimulation are completely suppressed in subjects when anesthetized with a MACEI95 (EI = endotracheal intubation) sevoflurane Hypothesis: The incidence of apnea with laryngospasm evoked by laryngeal stimulation will be reduced by 20% (from 25% to 5%) when the end-tidal concentration of sevoflurane is increased from 2.5% (MAC50) to 4.7% (MACEI95)Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University Hospital, Basel, SwitzerlandTreatments:
Sevoflurane
Criteria
Inclusion Criteria:- ASA I + II
- Elective intervention under general anesthesia
Exclusion Criteria:
- Reactive airway disease
- Respiratory tract infection (previous 2 weeks)
- Malignant hyperthermia
- Neuromuscular disease
- Cardiac disease