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Effects of etomidate, propofol and etomidate combined with propofol on hemodynamic changes in high blood pressure patients

Investigating the effects of etomidate, propofol and etomidate combined with propofol injections on hemodynamic changes in high blood pressure patients who are candidates for general anesthesia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231222060494N1
Enrollment
150
Registered
2024-01-07
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Hemodynamic status. Elevated blood-pressure reading, without diagnosis of hypertension

Interventions

Intervention 1: Intervention group: The group receiving propofol 1.5-2 mg/kg (Tehran shimi Co). Intervention 2: Intervention group: The group receiving etomidate 0 3 mg/kg (Aboreihan Co). Intervention

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with blood pressure between 140/80 and 170/90 are candidates for abdominal surgery

Exclusion criteria

Exclusion criteria: Patients with hemodynamic disorder who need therapeutic fluid and vasopressor.

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: The first, fifth and tenth minutes after induction. Method of measurement: Vital signs monitoring device.

Secondary

MeasureTime frame
Pulse rate. Timepoint: The first, fifth and tenth minutes after induction. Method of measurement: Vital signs monitoring device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayye Najafpour

Ardabil University of Medical Sciences

drsomayye@gmail.com+98 45 3323 2520

Outcome results

None listed

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