WithdrawnPhase 2ketamine

Compare the Effect of Propofol vs. "Ketofol" on Hemodynamic Stability During Induction of General Anesthesia

Sponsored by Yale University

NCT ID
NCT02282891
Start Date
2015-01
Est. Completion
2016-08

About This Study

The purpose of this study is to compare the hemodynamic effects of a standardized induction of general anesthesia with either propofol or ketofol in patients with physical status classification ASA 3. The study will be a double blinded, randomized controlled trial (RCT) with two arms of treatment groups. One arm will consist of induction of general anesthesia using a mixture of 1.5mg/kg:0.75mg/kg Propofol/ketamine (ketofol) and the induction dose will be 1.5mg/kg of propofol and 0.75mg/kg of ketamine; the second arm will consist of induction of general anesthesia using propofol 2mg/kg. The primary outcome of the intervention will consist of hemodynamic changes during the first 30 minutes after induction of general anesthesia.

Conditions Studied

Patients With "ASA 3" Designation

Interventions

  • Propofol
  • Propofol-Ketamine

Eligibility

Age:18 Years - 80 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients age 18-80 scheduled for elective surgery
* Physical status ASA 3.

Exclusion Criteria:

* Patients with a physical status of ASA 1,2, 4 or 5,
* Prior adverse reaction to propofol, ketamine or both

Study Locations (1)

Yale New Haven Hospital
New Haven, Connecticut, United States

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source