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Comparison of the Hemodynamic parameters of two regimens propofol-ketamin & etomidate during anesthesia induction in low EF CABG patients

Comparison of the Hemodynamic parameters of two regimens propofol-ketamin & etomidate during anesthesia induction in low EF CABG patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207184365N14
Enrollment
80
Registered
2012-11-07
Start date
2012-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodynamic Change. Postprocedural disorder of circulatory system, unspecified

Interventions

Intervention 1: Control group: Normal saline + 0.2 mg/kg Etomidate. Intervention 2: Intervention group: 1 mg/kg Ketamine + 1.5 mg/kg Propofol.
Treatment - Drugs
Control group: Normal saline + 0.2 mg/kg Etomidate
Intervention group: 1 mg/kg Ketamine + 1.5 mg/kg Propofol

Sponsors

Vice chancellor for research of Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: First time elective CABG surgery; Age between 40 and 70 years; EFMAP>110 mmHg; CABG with valve operation; Received etomidate or propofol or thiopental in one week ago; Egg and soy allergy; Sensitivity to etomidate or propofol or ketamine; Adrenal insufficiency

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mean arterial pressure. Timepoint: Before laryngoscopy as well as immediately, 1, 2 and 3 min after tracheal intubation. Method of measurement: Invasive Blood Pressure.;Systolic blood pressure. Timepoint: Before laryngoscopy as well as immediately, 1, 2 and 3 min after tracheal intubation. Method of measurement: Invasive Blood Pressure.;Diastolic blood pressure. Timepoint: Before laryngoscopy as well as immediately, 1, 2 and 3 min after tracheal intubation. Method of measurement: Invasive Blood Pressure.;Heart rate. Timepoint: Before laryngoscopy as well as immediately, 1, 2 and 3 min after tracheal intubation. Method of measurement: Heart monitoring.

Secondary

MeasureTime frame
Muscle twitching. Timepoint: After anesthetic infusion. Method of measurement: Inspection.;Pain on injection. Timepoint: After anesthetic infusion. Method of measurement: Inspection.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfshin Gholipour Baradari, MD

Mazandaran University Of Medical Sciences

gholipourafshin@mazums.ac.ir; gholipourafshin@yahoo.com+98 15 1222 6262

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026