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Ivabradine for Heart Failure (PROBE-IT Trial)
PROBE-IT Trial Summary
This trialinvestigates if ivabradine, a heart-rate reducing drug, can improve ventricular function in HFrEF patients unresponsive to beta-blocker therapy. It aims to reduce mortality and hospitalization rates in these patients.
- Systolic Heart Failure
- Dilated Cardiomyopathy
- Ventricular Remodeling
- Electrical Remodeling
PROBE-IT Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.PROBE-IT Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
To what extent is enrollment available for this medical experiment?
"Unfortunately, this trial is not accepting new patients at the time. It was first posted on November 1st 2016 and last updated on October 31st 2022. If you are searching for other studies related to ventricular remodeling, there are presently 215 clinical trials enrolling participants; conversely, 8 research studies related to Ivabradine require volunteers."
What conditions is Ivabradine most frequently prescribed for?
"Ivabradine is frequently used to provide relief from congestive heart failure, but can also be taken to manage symptoms of coronary artery disease (CAD), left ventricular dysfunction, and chronic stable heart failure."
Are there still open slots for people to join this research?
"Clinicaltrials.gov lists this medical trial as inactive; its initial posting was on November 1st 2016, and it last received an update in October 2022. However, there are currently 223 other trials that need patients to partake in them."
What other research has been done recently to explore the effects of Ivabradine?
"First investigated by the Chair of Cardiology in 2010, Ivabradine has since been studied 18350 times. Currently 8 active trials are ongoing with several based out of Columbus, Ohio."
Has Ivabradine received its regulatory go-ahead from the FDA?
"Ivabradine's safety is highly regarded and scored a 3; this drug has been approved, which justifies its inclusion in Phase 4 trials."
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