propofol with ketamine or propofol with etomidate, which one influences the hemodynamic stability lesser?

Phase 2

Conditions: Condition 1: Change in heart rate caused by anesthesia induction. Condition 2: Change in blood pressure caused by anesthesia induction.
Bradycardia, unspecified
Hypotension, unspecified

Registration Number: IRCT201112224731N10

Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 60

Inclusion Criteria

to have indication for elective surgeries; to be 50 or over 50 years old. Exclusion criteria: to have indication for emergency surgery; addiction to opiate; pregnancy; patients being treated with sedative or antipsychotic drugs in the past month; to have a personality disorder; to have body weight more than 20% of the ideal body weight for that height and gender; to have contraindication for etomidate, ketamine and propofol

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Systolic blood pressure. Timepoint: Before and immediately after induction, 1 and 3 minutes after intubation. Method of measurement: Non-invasive monitoring device with automatic cuff.;Heart rate. Timepoint: before and immediately after induction, 1 and 3 minutes after intubation. Method of measurement: Continuous ECG monitoring.;Blood O2 saturation. Timepoint: before and immediately after induction, 1 and 3 minutes after intubation. Method of measurement: pulse oximetry.;Diastolic blood pressure. Timepoint: before and immediately after induction, 1 and 3 minutes after intubation. Method of measurement: Non-invasive monitoring device with automatic cuff.;Mean arterial blood pressure. Timepoint: before and immediately after induction, 1 and 3 minutes after intubation. Method of measurement: non-invasive monitoring devices with automatic cuff.

Secondary Outcome Measures