Heart Rate Changes With Propofol

Completed

• Conditions: Surgical Patients
• Interventions: Other: Observation

• Registration Number: NCT01355432
• Lead Sponsor: Nationwide Children's Hospital

Brief Summary

This is a prospective pilot study to quantify the changes in heart rate when propofol is administered after inhalational anesthesia induction.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-05
• Study First Submitted: 2011-05-17
• Study First Submitted QC: 2011-05-17
• Study First Posted: 2011-05-18
• Status Verified: 2012-05
• Primary Completion: 2012-05
• Study Completion: 2012-05
• Last Update Submitted: 2012-05-01
• Last Update Posted: 2012-05-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

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.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Propofol	Observation	-

Primary Outcome Measures

Name	Time	Method
Change in heart rate	Baseline & every 30 secs for 3 mins

Trial Locations

Locations (1)

Nationwide Children's Hospital; 🇺🇸 Columbus, Ohio, United States