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OpenTrials
Completed

NCT Number: NCT01355432

Heart Rate Changes With Propofol

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

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Key information

Conditions

Surgical Patients

Age range

1 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Nationwide Children's Hospital

Columbus, Ohio, 43205, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 1 year of age or older.
  • Routine (elective) surgical patients with ASA classifications of 1 or 2 (healthy).
  • Patients that are already scheduled to receive inhalational induction followed by IV propofol.

Exclusion criteria

  • Premature infants of less than 30 weeks, who are less that 60 weeks post-gestational age at the time of study.

Treatment and study plan

observation

Other

There is no intervention, this is an observational study.

Primary outcomes

  1. Change in heart rate

    Time frame: Baseline & every 30 secs for 3 mins

Sponsors and collaborators

Lead sponsor

Nationwide Children's Hospital

Other

Registry information

Official study title

Changes in Heart Rate Following Administration of Propofol After Inhalational Induction

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
May 18, 2011
Registry last updated
May 2, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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