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Heart Rate Changes With Propofol

Nationwide Children's Hospital logo

Nationwide Children's Hospital

Status

Completed

Conditions

Surgical Patients

Treatments

Other: Observation

Study type

Observational

Funder types

Other

Identifiers

NCT01355432
IRB11-00236

Details and patient eligibility

About

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

Enrollment

40 patients

Sex

All

Ages

1+ year old

Volunteers

No Healthy Volunteers

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.

Trial design

40 participants in 1 patient group

Propofol
Treatment:
Other: Observation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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