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Studying the effects of two different hypnotic agents (Propofol & Etomidate) on relaxation function of left heart

Effect of Intravenous Propofol Versus Etomidate on Components of Left Ventricular Diastolic Function A Double Blinded, Randomized, Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034090
Enrollment
168
Registered
2021-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Pharmacological Intervention: Studying the effect of Propofol on diastolic function of left heart in patients undergoing surgery under general anaesthesia
2 mg per kg of propofol will be administered via Intravenous route over the span of 30 seconds Control Intervention1: Pharmacological Intervention: Studying the effect of Etomidate on diastolic functi
0.3 mg per kg of Etomidate will be administered via Intravenous route over the span of 30 seconds

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients ( >18 years of age) with ASA PS 1 or 2 requiring surgery under general anaesthesia will be recruited in this study

Exclusion criteria

Exclusion criteria: Patients with pre-existing cardiac lesions will be excluded from this study.

Design outcomes

Primary

MeasureTime frame
Comparison of the changes in E/e prime between the groupsTimepoint: After administration of the study drug, E/e prime will be measured and its change with baseline (before administration of the study drug) will be studied.

Secondary

MeasureTime frame
1) Comparison of change in e prime velocities between the groups 2) Comparison of change in E/A between the groups 3) Comparison of change in TRmax jet velocity between the groups 4) Comparison of change in LA volume indices be-tween the groups 5) Comparison of change in deceleration time between the groupsTimepoint: After the administration of the study drug, changes in the aforementioned parameters from the baseline will be studied

Countries

India

Contacts

Public ContactSenthilnathan Muthapillai

Jawaharlal Institute of Postgraduate Medical Education and Research

mmc.senthil@gmail.com7598566983

Outcome results

None listed

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