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Comparison of the Hemodynamic Changes of two regimens propofol + ketamin and thiopental Na + ketamin with etomidate during anesthesia induction

Comparison of the Hemodynamic Changes of two regimens propofol + ketamin and thiopental Na + ketamin with etomidate during anesthesia induction

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103114365N7
Enrollment
120
Registered
2011-07-10
Start date
2011-04-04
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

Treatment - Drugs
Intervention 1: Control group: Normal saline + 0.3 mg/kg Etomidate. Intervention 2: Intervention group 1 : 0.5 mg/kg Ketamine + 1.5 mg/kg Propofol. Intervention 3: Intervention group 2 : 0.5 mg/kg Ket
Control group: Normal saline + 0.3 mg/kg Etomidate
Intervention group 1 : 0.5 mg/kg Ketamine + 1.5 mg/kg Propofol
Intervention group 2 : 0.5 mg/kg Ketamine + 3 mg/kg thiopental Na

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Informed written consent; ASA class ?-??; Age between 18 and 45 years; Elective surgery Exclusion criteria: Adrenal insufficiency; Received etomidate or propofol or thiopental in one week ago; Receiving steroids at 6 months ago; Sensitivity to etomidate or propofol or thiopental; Egg and soy allergy; Sepsis; endocarditis; Chronic inflammatory diseases; Any severe disease and seriously endocrine, neurological, Psychiatric and Metabolic disorders; Pregnant or lactating women; Need for rapid intubation in emergency patients; Asthma; HIV infection; History of hypertension; Taking beta blocker, calcium blockers and angiotensin II inhibitors.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure. Timepoint: 1 min after administration of hypnotic drugs just before laryngoscopy as well as 1 and 3 min after laryngoscopy and tracheal intubation. Method of measurement: Automated sphygmomanometer.;Diastolic blood pressure. Timepoint: 1 min after administration of hypnotic drugs just before laryngoscopy as well as 1 and 3 min after laryngoscopy and tracheal intubation. Method of measurement: automated sphygmomanometer.;Mean arterial pressure. Timepoint: 1 min after administration of hypnotic drugs just before laryngoscopy as well as 1 and 3 min after laryngoscopy and tracheal intubation. Method of measurement: automated sphygmomanometer.;Heart rate. Timepoint: 1 min after administration of hypnotic drugs just before laryngoscopy as well as 1 and 3 min after laryngoscopy and tracheal intubation. Method of measurement: Heart monitoring.

Secondary

MeasureTime frame
Delirium. Timepoint: After anesthesia. Method of measurement: Inspection.;Nausea and vomiting. Timepoint: After anesthesia. Method of measurement: Inspection.;Twitching. Timepoint: After anesthetic infusion. Method of measurement: Inspection.;Pain. 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 15132612458

Outcome results

None listed

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