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

PHASE4RecruitingINTERVENTIONAL
Enrollment

172

Participants

Timeline

Start Date

June 1, 2023

Primary Completion Date

December 31, 2024

Study Completion Date

March 31, 2025

Conditions
SepsisIvabradineHemodynamicsHeart Rate Control
Interventions
DRUG

Ivabradine

After randomization, the starting dose of ivabradine, 5mg, is given via the gastrointestinal tract every 12 hours. Heart rate control ranged from 70 to 94 bpm. Ivabradine was maintained until 96 hours after initiation of therapy. Beyond this period, the decision to continue ivabradine is left to the discretion of the treating intensivist. During the drug intervention period, heart rate is assessed before each dose. Ivabradine is tapered or discontinued if the heart rate is lower than the target rate; If the heart rate remains ≥95 bpm after 48 hours, the dose is increased to 7.5mg. If a heart rate of 95 or more bpm recurs after discontinuation during the intervention period, treatment with ivabradine can be resumed. Furthermore, Ivabradine is also discontinued at any time in the presence of severe liver impairment, malignant arrhythmia, cardiac conduction block, allergy, the need to take drugs with potentially harmful effects of ivabradine.

Trial Locations (1)

510260

RECRUITING

the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou

All Listed Sponsors
lead

Second Affiliated Hospital of Guangzhou Medical University

OTHER