Surgical Patients
Conditions
Brief summary
This is a prospective pilot study to quantify the changes in heart rate when propofol is administered after inhalational anesthesia induction.
Interventions
There is no intervention, this is an observational study.
Sponsors
Study design
Eligibility
Inclusion criteria
1. At least 1 year of age or older. 2. Routine (elective) surgical patients with ASA classifications of 1 or 2 (healthy). 3. Patients that are already scheduled to receive inhalational induction followed by IV propofol.
Exclusion criteria
1\. Premature infants of less than 30 weeks, who are less that 60 weeks post-gestational age at the time of study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in heart rate | Baseline & every 30 secs for 3 mins |
Countries
United States