Effect of Heart Rate Control With Ivabradine on Hemodynamic in Patients With Sepsis

Launched by SECOND AFFILIATED HOSPITAL OF GUANGZHOU MEDICAL UNIVERSITY · May 20, 2023

Keywords

ClinConnect Summary

This clinical trial is studying the effects of a medication called ivabradine on heart rate and blood flow in patients with sepsis, a serious condition caused by infections that can lead to organ failure. The goal is to see if controlling a fast heart rate (tachycardia) can improve outcomes for these patients, as high heart rates have been linked to increased risk of death. Ivabradine works by slowing down the heart rate without affecting the strength of the heart's contractions, which is a different approach compared to traditional medications like beta-blockers.

To participate in this study, patients need to be adults, at least 18 years old, and currently being treated in an intensive care unit for sepsis. They should have a stable blood pressure and a heart rate of 95 beats per minute or higher for at least two hours. Participants will be randomly assigned to receive either ivabradine or a placebo (a substance with no active medication) and will be monitored closely for changes in heart rate and blood flow. This trial is actively recruiting participants and aims to gather important information on how heart rate control can impact recovery in sepsis patients.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Adult patients aged 18 years or above.
• • 2. Being treated in an intensive care unit.
• • 3. Sepsis is diagnosed according to Sepsis-3.0 criteria, which is defined as patients requiring antimicrobial agents due to confirmed or suspected infection, acute increase in the SOFA score at least 2 points.
• • 4. Mean arterial pressure (MAP) is maintained ≥65 mmHg with adequate volume resuscitation and vasopressor therapy. Volume resuscitation is considered adequate when Central Venous Pressure (CVP) \> 8mmHg, global end-diastolic volume index (GEDI) \> 680ml/m2 and resting inferior vena cava (IVC) diameter \> 1.5cm.
• • 5. Patients are in a relatively stable period of hemodynamics, as defined that the targe mean arterial pressure are maintained with the same dosage of vasopressors for at least 2 h.
• • 6. Sinus rhythm with heart rate ≥ 95bpm maintain for at least 2 hours but less than 72 hours.
• Exclusion Criteria:
• • 1. Patients who had received ivabradine therapy or known allergy to it prior to randomization.
• • 2. Patients with severe liver dysfunction (Child-C grade).
• • 3. Patients with a history of pre-existing chronic renal failure (glomerular filtration rate less than 15 ml/min/1.73 m2), except patients treated with continuous renal replacement therapy (CRRT).
• • 4. Patients with known seizure disorder.
• • 5. Patients with any contraindication to gastrointestinal drug administration.
• • 6. Pregnant or lactating patients.
• • 7. patients requiring the use of potent cytochrome CYP3A4 inhibitors such as antifungals of the azole-type (specifically ketoconazole and itraconazole), macrolide antibiotics (specifically clarithromycin and erythromycin) and HIV protease inhibitors (specifically nelfinavir and ritonavir).
• • 8. Patients with active bleeding;
• • 9. Patients with cardiac dysfunction caused by non-septic causes such as recent (\< 2months) acute myocardial infarction, chronic cardiac dysfunction (NYHA Class Ⅳ), congenital heart disease, pericardial tamponade, severe aortic regurgitation and aortic coarctation before enrollment.
• • 10. Patients with sinoatrial block, sick sinus syndrome, atrioventricular block or heart rate dependence on pacemaker.
• • 11. Patients with refractory shock, which may be considered if one of the following conditions still exists in spite of active volume resuscitation, high doses of vasoactive drugs (VIS score \>120), and other regular therapy: 1) Worsening hypotension (MAP\<65mmHg); 2) Lactate persistence\>5mmol/L (two times in a row with an interval of more than 30min), and a progressive upward trend; 3) Mixed venous blood oxygen saturation (SvO2) sustained \<55% (more than two consecutive times, more than 30min apart), and progressive deterioration. The above conditions lasted for more than 5 hours.
• • 12. Use of beta blockers within 24 hours before enrollment.
• • 13. Pheochromocytoma patients.
• • 14. After cardiopulmonary resuscitation.
• • 15. Patients who have been enrolled in another interventional clinical study.