No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
65 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Other
Participants needed
18 (estimated)
Sponsor
Weill Medical College of Cornell University · Other
Who this trial is looking for
This trial is looking for older adults with heart failure who are taking beta-blockers. Participants will explore their options to continue or stop their medication through personalized testing.
Are You a Good Fit for This Trial?
Must be takingBeta-blocker
You may be able to join if
I am at least 65 years old.
I have heart failure with preserved ejection fraction.
I am taking a beta-blocker.
You may not be able to join if
I have severe aortic stenosis or severe mitral stenosis.
I have had a heart attack or heart surgery in the past 3 years.
I have unstable heart failure or have been hospitalized in the past 30 days.
I have moderate-severe dementia or a psychiatric disorder.
I have a life expectancy of less than 6 months.
I cannot provide informed consent.
I am enrolled in another clinical trial.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Investigators will determine whether N-of-1 trials, as a pragmatic, participant-centered approach to medication optimization that can overcome key barriers of deprescribing, can lead to increased participant confidence regarding their preference to continue or discontinue beta-blockers in older adults with Heart Failure with Preserved Ejection Fraction (HFpEF).
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
1. Ambulatory adults age ≥ 65 years with HFpEF, according to ACC/AHA guidelines (signs and symptoms of heart failure AND ejection fraction ≥ 50%)
2. Taking beta-blocker
Exclusion Criteria:
1. Alternate cause(s) of HFpEF Syndrome:
1. Severe aortic stenosis
2. Moderate-se…
Inclusion Criteria:
1. Ambulatory adults age ≥ 65 years with HFpEF, according to ACC/AHA guidelines (signs and symptoms of heart failure AND ejection fraction ≥ 50%)
2. Taking beta-blocker
Exclusion Criteria:
1. Alternate cause(s) of HFpEF Syndrome:
1. Severe aortic stenosis
2. Moderate-severe mitral stenosis
3. Constrictive pericarditis
4. High output HF
5. Infiltrative cardiomyopathy
2. Other compelling indication(s) for beta-blocker
1. Prior EF \< 50%
2. Hypertrophic cardiomyopathy
3. Angina
4. Acute coronary syndrome, myocardial infarction, or coronary artery bypass surgery in prior 3 years
5. History of ventricular tachycardia/arrhythmia
6. Atrial arrhythmia with hospitalization for rapid ventricular response, prior 1 year
7. Heart rate \>100 bpm within the prior 3 months
8. Atrial arrhythmia with ventricular rate \>90 per minute in the prior 3 months
9. Systolic blood pressure readings \>160 mmHg within the prior 3 months, unless classified as white coat hypertension/effect (and home blood pressures below 140 mmHg)
10. Non-cardiac indications (e.g., migraine prevention, anxiety symptom management, hyperthyroidism, essential tumor reduction)
3. Clinical instability (N-of-1 trials are appropriate for stable conditions only)
1. Decompensated heart failure
2. Hospitalization in the past 30 days
3. Medication changes or procedures in the prior 14 days that could confound observations/data at PI discretion
4. Anticipated medication changes or procedures in subsequent 3 months that could confound observations/data at PI discretion
5. Clinical instability from other medical issues
4. Estimated life expectancy \< 6 months
5. Moderate-severe dementia or psychiatric disorder precluding informed consent
6. Language barrier that will preclude informed consent and ability to comprehend study procedures
7. Non-compliance or inability to complete study procedures
8. Enrollment in a clinical trial not approved for co-enrollment
9. Any condition that, in the Principal Investigator or treating physician's opinion, makes the patient unsuitable for study participation
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