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NCT05265520Recruiting

His-Bundle Corrective Pacing in Heart Failure

Source: ClinicalTrials.gov · Last updated 9 Feb 2026

Brief summary (registry, in English)

The investigators aim to prospectively evaluate the efficacy and mechanism of benefit of His-bundle pacing enhanced cardiac resynchronization therapy (His-CRT) vs. cardiac resynchronization therapy (BIV-CRT) in patients with heart failure and right bundle branch block (RBBB).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
10 Feb 2022
Start date
2 Dec 2022
Primary completion date
1 Jul 2027
Lead sponsor
University of Rochester
NCT number
NCT05265520

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From 2 Dec 2022 to the primary completion date, 1 Jul 2027
  • 14 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Unable to obtain most recent imaging data from echocardiogram within 1 year prior to date of randomization

Other illness

  • On heart transplant list or likely to undergo heart transplant

Other

  • Left bundle branch block (LBBB) or intraventricular conduction delay (IVCD) ECG morphology
  • Unable or unwilling to follow study protocol
  • Less than 12 months life expectancy at consent
  • Pregnancy or planned pregnancy during duration of the study

Who the study is looking for

  • Age 18 years or older (no upper age limit)
  • Optimal medical therapy for heart failure by current guidelines
  • Class IIa or IIb guideline-based indication for CRT-D implant in RBBB patients, including one of the following:
    • New York Heart Association (NYHA) class II HF symptoms, LVEF ≤ 30% and QRS≥ 150 ms (IIb); OR
    • NYHA class III-IV a HF, LVEF ≤ 35%, and QRS duration ≥ 150 ms (IIa); OR
    • NYHA class III-IV a HF, LVEF ≤ 35%, and QRS duration 120-149 ms (IIb)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mission Health
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AshevilleUnited StatesRecruiting
University of Vermont
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BurlingtonUnited StatesRecruiting
Northwestern Memorial Hospital
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ChicagoUnited StatesRecruiting
Rush University Medical Center
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ChicagoUnited StatesRecruiting
University of Chicago
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ChicagoUnited StatesRecruiting
Cedars-Sinai Medical Center
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Los AngelesUnited StatesRecruiting
Mount Sinai Hospital
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New YorkUnited StatesRecruiting
Weill Cornell Medical College
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New YorkUnited StatesRecruiting
University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting
University of Arizona
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PhoenixUnited StatesRecruiting
Virginia Commonwealth University
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RichmondUnited StatesRecruiting
Valley Health System
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RidgewoodUnited StatesRecruiting
University of South Florida
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TampaUnited StatesRecruiting
Geisinger Wyoming Valley
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Wilkes-BarreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.