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NCT04767061 · ClinicalTrials.gov registry record · Phase 4

Impact of Beta-blockers on Physical Function in HFpEF

A Phase 4 study, sponsored by Weill Medical College of Cornell University.

Completed
Registry status
Phase 4
Development phase
9
Enrollment target

NCT04767061: Completed Phase 4 study, sponsored by Weill Medical College of Cornell University.

NCT04767061 is a Phase 4 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 9 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04767061, a Phase 4 study, has completed, sponsored by Weill Medical College of Cornell University.

COMPLETED
Registry status
Phase 4
Development phase
9 participants
Enrollment target

Study Summary

The purpose of this study is to understand the impact of beta-blockers on physical function in older adults with heart failure. We will achieve this objective by conducting N-of-1 trials. N-of-1 trials are personalized experiments that test different treatment options in an individual patient.

Primary Outcome

The wearable activity monitoring device measures daily step count. Due to the nature of N-of-1 trials, the duration of a subject's periods varies based on the subject's "home" dose of beta-blocker prior to enrollment, therefore, each subject's respective time period for the OFF and ON periods could range between 3 and 6 weeks. We will compare average step counts over 2-week periods, which will be the final 2 weeks of each period when subjects are either on their "home" (ON Beta Blockers) or mini

Interventions

  • DRUG Beta blockers

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2021-04-01
Est. Completion 2023-04-28
Phase Phase 4

What the finished NCT04767061 record still lists

NCT04767061 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Beta blockers is the first listed.

NCT04767061 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04767061 about?

NCT04767061 is a clinical study titled "Impact of Beta-blockers on Physical Function in HFpEF". The purpose of this study is to understand the impact of beta-blockers on physical function in older adults with heart failure. We will achieve this objective by conducting N-of-1 trials. N-of-1 trials are personalized experiments that test different treatment options in an individual patient.

What is the current status of trial NCT04767061?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 9 participants. The study started on 2021-04-01. Estimated completion is 2023-04-28.

What interventions are being tested in trial NCT04767061?

The interventions under investigation include: Beta blockers (DRUG).

Who is sponsoring clinical trial NCT04767061?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04767061's enrollment target sits among peer trials

9 1968th of 2000 higher than 29 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04767061, the US trial registry maintained by the National Library of Medicine. NCT04767061 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.