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comparison the effects of Etomidate and remifentanil on hemodynamic

Comparison the effects of etomidate and remifentanil induction on hemodynamic response in patients undergoing cataract surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220309054238N1
Enrollment
70
Registered
2022-04-18
Start date
2022-04-21
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Cataract.

Interventions

Intervention 1: Intervention group: patients will be divided in two groups.(each group will have 35 patients).in operating room vital signs will be monitored using a continuous electrocardiogram, non

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 86 Years

Inclusion criteria

Inclusion criteria: Patients with grade 1 and grade 2 physical status of ASA(American society of Anesthesiologists) Patients without cardiac disease Patients without chronic kidney disease Patients without metabolic disease Patients without known hypersensitivity reaction to Etomidate and Remifentanil patients who provide informed consent

Exclusion criteria

Exclusion criteria: cardiac arrest during surgery or recovery patients who didn't provide consent

Design outcomes

Primary

MeasureTime frame
Mean Arterial pressure Which is the average arterial pressure throughout one cycle. Timepoint: measuring blood pressure right after induction and in 5,10,15,20 minutes after induction(during surgery). Method of measurement: Measuring blood pressure with vital sign monitoring device during surgery.(Non-invasive blood pressure measuring).;Pulse rate. Timepoint: measuring Pulse rate right after induction and in 5,10,15,20 minutes after induction(during surgery). Method of measurement: Measuring pulse rate with vital sign monitoring device during surgery.(ECG/Resp ).;Respiratory rate. Timepoint: measuring Respiratory rate right after induction and in 5,10,15,20 minutes after induction(during surgery). Method of measurement: Measuring respiratory rate with vital sign monitoring device during surgery.(ECG/Resp ).

Secondary

MeasureTime frame
Pain score. Timepoint: After Surgery(in recovery room). Method of measurement: Visual Analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPooria Ghadimi

Arak University of Medical Sciences

Pooria_ghadimi@yahoo.com+98 86 3312 4889

Outcome results

None listed

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