The Hypotensive Effect of Propofol: an Observational Study

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Penn State Health

Status

Completed

Conditions

Hypotension
Anesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT01508351
38444

Details and patient eligibility

About

Hypotension is a recognized frequent complication of induction of anesthesia. The intent of this research is to determine the incidence of hypotension in patients receiving anesthetic induction with propofol. This investigation seeks to examine how normal clinical practice or a "real world" understanding of the usual response to propofol affects hemodynamics without isolating or standardizing other variables. The current research concerns hypotension in normal clinical practice where variability exists. This project aims to gather information and data in an attempt to form a foundation upon which each of the other variables affecting blood pressure may be subsequently assessed.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All ASA 1-3 patients who are to receive propofol induction for general anesthesia

Exclusion criteria

  • Allergy to propofol
  • ASA 4 and above

Trial design

100 participants in 1 patient group

Propofol Induction
Description:
All patients receiving propofol induction of anesthesia who are ASA 1-3

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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