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NCT06678841 · ClinicalTrials.gov registry record · NA

ELEVATE-HFpEF Clinical Study

A NA study of Heart Failure With Preserved Ejection Fraction (HFPEF), sponsored by Medtronic Cardiac Rhythm and Heart Failure.

Recruiting
Registry status
NA
Development phase
700
Enrollment target
20
Study locations

NCT06678841: Recruiting NA study of Heart Failure With Preserved Ejection Fraction (HFPEF), sponsored by Medtronic Cardiac Rhythm and Heart Failure.

NCT06678841 is a NA study of Heart Failure With Preserved Ejection Fraction (HFPEF) that is actively recruiting participants, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 700 participants, above the 142-participant average among 9 other Heart Failure With Preserved Ejection Fraction (HFPEF) trials with a reported enrollment target (393% higher). The trial reports 20 study locations across 17 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06678841, a NA study of Heart Failure With Preserved Ejection Fraction (HFPEF), is actively recruiting participants, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

RECRUITING
Registry status
NA
Development phase
700 participants
Enrollment target
20
Study locations

Study Summary

ELEVATE-HFpEF is a prospective, randomized, controlled, double-blinded, multi-center, global, interventional pivotal study evaluating the safety and efficacy of dual chamber personalized pacing compared to minimal or no pacing for the treatment of patients with heart failure with preserved ejection fraction (HFpEF).

Primary Outcome

Cardiovascular mortality, urgent heart failure events, and ODI heart failure events will be collected as they occur. The Kansas City Cardiomyopathy Questionnaire (KCCQ); (range of score is 0 to 100), 6-minute walk test (distance in meters), and N-terminal pro-B-type natriuretic peptide (NT-proBNP) (picograms per milliliter, pg/mL) will be collected at Baseline and the 12-months visit. Treatment and control groups will be compared using a win ratio.

Interventions

  • DEVICE Personalized cardiac pacing

Study Locations (20)

Other

  • Ordensklinikum Linz GmbH / Elisabethinen - Linz
  • Universitair Ziekenhuis Antwerpen - Edegem
  • Centre Hospitalier Universitaire Besancon - Hôpital Jean Minjoz - Besançon

Ohio

  • The Ohio State University Wexner Medical Center - Columbus
  • Mount Carmel East - Columbus

Connecticut

  • Hartford Hospital - Hartford

Florida

  • Cardiovascular Institute of Northwest Florida - Panama City

Georgia

  • Emory University - Atlanta

Iowa

  • Iowa Heart Center - Des Moines

Louisiana

  • Cardiovascular Institute of the South - Houma

Missouri

  • Saint Lukes Mid America Heart Institute - Kansas City

Trial Details

FieldValue
Enrollment Target 700 participants
Start Date 2025-07-09
Est. Completion 2029-02
Phase NA

What NCT06678841 shows while recruiting

NCT06678841 is an interventional study that assigns participants to a tested intervention. The registered 700 participants enrollment target is mid-sized for trials with a published cap, above the 142-participant average among 9 other Heart Failure With Preserved Ejection Fraction (HFPEF) trials with a reported enrollment target (393% higher).

The record links to 1 condition, with Heart Failure With Preserved Ejection Fraction (HFPEF) appearing as the primary indexed condition, and to 1 intervention - of which Personalized cardiac pacing is the first listed.

NCT06678841 names 20 study sites across 17 states, led by Other, Ohio, Connecticut.

Frequently Asked Questions

What is clinical trial NCT06678841 about?

NCT06678841 is a clinical study titled "ELEVATE-HFpEF Clinical Study". ELEVATE-HFpEF is a prospective, randomized, controlled, double-blinded, multi-center, global, interventional pivotal study evaluating the safety and efficacy of dual chamber personalized pacing compared to minimal or no pacing for the treatment of patients with heart failure with preserved ejection ...

What is the current status of trial NCT06678841?

This trial is currently recruiting. It is a NA study. The enrollment target is 700 participants. The study started on 2025-07-09. Estimated completion is 2029-02.

What conditions does trial NCT06678841 study?

This clinical trial studies the following conditions: Heart Failure With Preserved Ejection Fraction (HFPEF).

What interventions are being tested in trial NCT06678841?

The interventions under investigation include: Personalized cardiac pacing (DEVICE).

Who is sponsoring clinical trial NCT06678841?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 115 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06678841 being conducted?

This trial has 20 study locations across Connecticut, Florida, Georgia, Iowa, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Heart Failure With Preserved Ejection Fraction (HFPEF)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06678841's enrollment target sits among peer trials

700 1st of 9 higher than 9 of 9 other Heart Failure With Preserved Ejection Fraction (HFPEF) trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Heart Failure With Preserved Ejection Fraction (HFPEF) 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 NCT06678841, the US trial registry maintained by the National Library of Medicine. NCT06678841 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.