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Ivabradine in controlling elevated heart rate among sick patients

Ivabradine in controlling tachycardia among critically ill patients - None

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2010/091/002969
Enrollment
100
Registered
2011-02-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Sinus Tachycardia

Interventions

Intervention1: Ivabradine: 7.5 mg, Per-oral or via NG Tube, 2 doses at 12 hours apart Control Intervention1: Pantoprazole: 40 mg, Per-oral or via NG Tube, 2 doses at 12 hours apart.

Sponsors

Fluid Research Grant Christian Medical CollegeVellore Tamilnadu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a)Aged above 18 years b)Sinus rhythm with heart rate above 120 bpm c) 24 hours of admission to the ICU with a diagnosis of shock. d)In case of patients admitted with Organophosphorus poisoning, they should have been off atropine for at least 48 hours.

Exclusion criteria

Exclusion criteria: ICU Physician assessment Sick sinus syndrome Sinu-atrial block Pacemaker-dependency 3rd degree AV block Ongoing fluid/volume loss On concomitant use of potent CYP3A4 inhibitors: Azole antifungals (ketoconazole, itraconazole), Clarithromycin , erythromycin, josamycin, telithromycin, HIV protease inhibitors (nelfinavir, ritonavir)

Design outcomes

Primary

MeasureTime frame
Comparison of the mean heart rate between the treatment and control group 24 hours after the initiation of the treatment.Timepoint: 24 hours

Secondary

MeasureTime frame
Hemodynamic parameters up to 24 hrs. Blood pressure and Mean Arterial Pressure (mm of Hg) Urine output (ml/ hour) Estimated Glomerular Filtration Rate (eGFR) Blood lactate levels P:F ratio Duration of ventilation days MortalityTimepoint: 24 hours

Countries

India

Contacts

Public ContactDr Shubhanker Mitra
kurien123@gmail.com04162282166

Outcome results

None listed

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