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Comparison of hemodynamic response to laryngoscopy and endotracheal intubation in induction of general anesthesia with Propofol, Sodium thiopental, Etomidate, Propofol-Etomidate and Propofol- Sodium thiopental combination

Comparison of hemodynamic response to laryngoscopy and endotracheal intubation in induction of general anesthesia with Propofol, Sodium thiopental, Etomidate, Propofol-Etomidate and Propofol- Sodium thiopental combination

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251107067899N1
Enrollment
195
Registered
2025-11-13
Start date
2025-12-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Cardiovascular complications and hemodynamic changes in patients under general anesthesia. Encounter for other preprocedural examination

Interventions

Intervention 1: Intervention group: Propofol (2 mg/kg), intravenous emulsion, administered as an IV bolus for anesthesia induction immediately after pre-oxygenation and initial fluid administration. T

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: ASA1 & ASA2 patients Patients who are candidates for short elective surgeries (lasting less than two hours) under general anesthesia

Exclusion criteria

Exclusion criteria: History of general anesthesia within the past six months Pregnant women Patients with poorly controlled diabetes mellitus Patients with poorly controlled chronic obstructive pulmonary disease (COPD) Chronic use of analgesic or sedative medications Uncontrolled hypertension or cardiovascular disease, or prolonged use of beta-adrenergic blocking agents Predicted difficult airway management (Mallampati classification = III) History of hypersensitivity or allergic reaction to anesthetic agents used History of porphyria Body mass index (BMI) greater than 25 kg/m²

Design outcomes

Primary

MeasureTime frame
Heart Rate. Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Cardiac Monitoring.;Systolic Blood Pressure. Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Measured in millimeters of mercury (mmHg) using a calibrated sphygmomanometer.;Dyastolic Blood Pressure. Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Measured in millimeters of mercury (mmHg) using a calibrated sphygmomanometer.;Arterial oxygen saturation (SpO2). Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Pulse Oxymeter.

Secondary

MeasureTime frame
Hypotension. Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Calibrated sphygmomanometer.;Bradycardia. Timepoint: Before drug administration, at 1 and 3 minutes after induction of anesthesia, and at 1, 3, 5, and 10 minutes after intubation. Method of measurement: Cardiac monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDaryoosh Moradi Farsani

Esfahan University of Medical Sciences

Dmoradi@med.mui.ac.ir+98 31 3620 1992

Outcome results

None listed

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