CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 50 enrolled
Drug / intervention
Amlodipine Besylate +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04434664
NCT04434664Phase 4Completed

BLOCKade of Calcium Channels and Beta Adrenergic Receptors for the Treatment of Hypertension in Heart Failure With Preserved Ejection Fraction (BLOCK HFpEF) Trial

University of Pennsylvania·interventional·Posted Jun 17, 2020·Updated Jan 30, 2026

In Brief

A Phase 4 clinical trial evaluating Amlodipine Besylate and Metoprolol Succinate for Heart Failure With Preserved Ejection Fraction and Hypertension. Completed, enrolled 50 participants across 1 site.

Detailed Summary

Heart failure with preserved ejection fraction (HFpEF) is a critical public health problem. Heart failure (HF) affects over 5 million adults in the United States (US), and is a major source of morbidity, mortality, and impaired quality of life. Approximately half of individuals with HF have a preserved left ventricular (LV) ejection fraction (EF), termed HF with preserved EF (HFpEF). While there are several effective pharmacologic therapies for HF with reduced ejection fraction (HFrEF), none have been identified for HFpEF. Hypertension, which is present in approximately 80% of individuals with HFpEF, is the foremost modifiable risk factor for the development and progression of HFpEF. Despite the clinical importance of hypertension in HFpEF, there is limited information on how common antihypertensive agents, particularly calcium channel blockers (CCBs) and β-blockers, effect pathophysiologic mechanisms of HFpEF. This is a mechanistic investigation of the role of dihydropyridine CCBs compared to β-blockers (commonly used antihypertensive agents in clinical practice) in targeting key physiologic abnormalities in HFpEF.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
202120222023202420252026
First PostedJun 17, 2020
Enrollment StartDec 1, 2021
Primary CompletionDec 3, 2024
Study CompletionDec 20, 2024
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 6.0 years ago

Interventions

Amlodipine Besylatedrug

The interventions will be implemented in random order in a crossover (AB-BA) design, separated by an approximately one-week washout period

Metoprolol Succinatedrug

The interventions will be implemented in random order in a crossover (AB-BA) design, separated by an approximately one-week washout period