Overview

Sevoflurane and Laryngeal Reflex Responses in Pediatric Patients

Status:
Terminated
Trial end date:
2008-08-01
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Hospital, Basel, Switzerland
Treatments:
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