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Beta-adrenergic Agonist

Inhaled Beta-adrenergic Agonists to Treat Pulmonary Vascular Disease in Heart Failure With Preserved EF (BEAT HFpEF): A Randomized Controlled Trial (BEAT HFpEF Trial)

Phase 3
Waitlist Available
Led By Barry A Borlaug, MD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 10 minutes after intervention during exercise
Awards & highlights
All Individual Drugs Already Approved
Approved for 10 Other Conditions
Pivotal Trial

Summary

The enormous and rapidly growing burden of Heart Failure with Preserved Ejection Fraction (HFpEF) has led to a need to understand the pathogenesis and treatment options for this morbid disease. Recent research from the investigator's group and others have shown that pulmonary hypertension (PH) is highly prevalent in HFpEF, and right ventricular (RV) dysfunction is present in both early and advanced stages of HFpEF. These abnormalities in the RV and pulmonary vasculature are coupled with limitations in pulmonary vasodilation during exercise. There are no therapies directly targeted at the pulmonary vasculature that have been clearly shown to be effective in HFpEF. A recent study by Mayo Clinic Investigators has demonstrated pulmonary vasodilation with dobutamine (a beta 2 agonist) in HFpEF. As an intravenous therapy, this is not feasible for outpatient use. In the proposed randomized, placebo-controlled double blinded trial, the investigators seek to evaluate whether the commonly used inhaled bronchodilator albuterol (a beta 2 agonist), administered through a high-efficiency nebulizer device that achieves true alveolar drug delivery, improves pulmonary vascular resistance (PVR) at rest and during exercise in patients with HFpEF as compared to placebo. This has the potential to lead to a simple cost effective intervention to improve symptoms in HFpEF, and potentially be tested in other World Health Organization (WHO) Pulmonary Hypertension groups. PVR is an excellent surrogate marker for pulmonary vasodilation and has been used in previous early trials of PH therapy.

Eligible Conditions
  • Congestive Heart Failure
  • Heart Failure

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 10 minutes after intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 10 minutes after intervention for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in 20 Watt Exercise Pulmonary Vascular Resistance (PVR)
Secondary study objectives
Change in Exercise Cardiac Output
Change in Exercise Pulmonary Artery Compliance
Change in Exercise Pulmonary Artery Pressure
+10 more

Awards & Highlights

All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 10 Other Conditions
This treatment demonstrated efficacy for 10 other conditions.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Inhaled albuterolExperimental Treatment1 Intervention
2.5 mg inhaled albuterol through a high efficiency nebulizer -single dose
Group II: Inhaled saline placeboPlacebo Group1 Intervention
Inhaled saline through a high efficiency nebulizer -single dose
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Salbutamol
FDA approved

Find a Location

Who is running the clinical trial?

Mayo ClinicLead Sponsor
3,355 Previous Clinical Trials
3,061,743 Total Patients Enrolled
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,941 Previous Clinical Trials
47,792,889 Total Patients Enrolled
Barry A Borlaug, MDPrincipal InvestigatorMayo Clinic
2 Previous Clinical Trials
96 Total Patients Enrolled
~3 spots leftby Dec 2025