Skip to content

Comparison between oral Ivabradine and Intravenous Esmolol for their efficacy in achieving pressor response during intubation, in ASA grade I patients

Attenuation of pressor response to laryngoscopy and endotracheal intubation with oral Ivabradine versus intravenous Esmolol in American society of Anesthesiologist physical status grade I patients - Open label randomised control trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078154
Enrollment
60
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: H948- Other specified disorders of ear in diseases classified elsewhere

Interventions

Intervention1: IVABRADINE: Ivabradine is administered orally at a dosage of 5mg, 2 hours before endotracheal intubation.It selectively inhibits the If current in the sinoatrial node, reducing heart ra

Sponsors

Government medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a.American Society of Anesthesiologists (ASA) –Physical Status grade I b.Patients with Mallampatti class I and II c.Patients with Normal ECG d.Patients Scheduled for elective non- cardiac surgery requiring endotracheal intubation.

Exclusion criteria

Exclusion criteria: a.Patients refusal or not consented to participate in the study. b.Patient with previous H/O Chest Pain/ Palpitations/Syncope c.Patient with H/o Respiratory Problems d.Patient with Hepatic or renal Problems e.Patient with Known allergies to Esmolol or Ivabradine f. Patient with History of cardiac conduction abnormalities. g.Patient with ECG abnormalities h.Patient with difficult airway i.Patient with Heart rate less than 60/minute and Systolic blood pressure less than 100mmHg j.Patient with total duration of laryngoscopy and intubation more than 20 seconds k.Patient with Mallampatti class III and IV Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Mean Heart rate, Mean Systolic blood pressure Mean diastolic blood pressureTimepoint: At base level, after study drug, after induction, after intubation, 1st minute, 3rd minute, 5th minute, 8th minute, 10th minute, 1st hour and 2nd hour

Secondary

MeasureTime frame
Adverse drug reactionTimepoint: after 12 hours of study drug

Countries

India

Contacts

Public Contactsundharalingam senthilraj

government medical college, nalgonda.

nasertadvi@yahoo.co.uk9052734381

Outcome results

None listed

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