Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating His Bundle Pacing for Heart Conditions

Official title: His Bundle Pacing in Bradycardia and Heart Failure

Run by Mayo Clinic · NCT03008291 · Data updated 2026-11-12

This study is testing if special pacing techniques during pacemaker implantation can help improve heart function in people with heart failure or slow heart rates.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorMayo Clinic
Academic / other
Locations1 site (Rochester, Minnesota)
StatusRecruiting
StartedOctober 2016
Main results expectedDecember 2026
Study endsDecember 2026
Registry record updatedDecember 24, 2025
Trial IDNCT03008291 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients with heart failure scheduled for pacemaker implantation or those with AV block or bradycardia recommended for dual chamber pacemaker implantation.

Probably not a fit

Patients under 18 years old or pregnant women will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on patients with heart failure or bradycardia who are scheduled for pacemaker implantation. Participants will undergo procedures such as His bundle pacing or left bundle area pacing, and additional heart rhythm measurements will be collected during the implantation to assess the effects on electrical conduction. The study aims to understand how these pacing techniques can normalize atrioventricular conduction in patients with heart failure or AV block.

Why it matters

Potential benefit: If successful, this study could lead to improved pacing techniques that enhance heart function and patient outcomes in those with heart failure and bradycardia.

How similar studies have gone: Other studies have shown promising results with similar pacing approaches, indicating potential for success in this area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

HF Group

* Clinically recommended to undergo PM, CRT-P, or CRT-D implantation or HIBP/LBAP (including HIBP/LBAP for patients with HF, for patients who have failed CRT implant or patients who are CRT non-responders)
* Any QRS duration
* LVEF ≤ 50%

AV Block/Bradycardia Group

* Recommended to undergo dual chamber pacemaker implantation
* Any AV block or Sinus Bradycardia

Exclusion Criteria:

* Age \< 18 years
* Pregnant

Where it's running

  • Mayo Clinic
    Rochester, Minnesota, United States
    Recruiting

Study contacts

  • Principal investigator: Yong-Mei Cha, M.D. — Mayo Clinic
  • Study coordinator: Yong-Mei Cha, M.D.
  • Email: ycha@mayo.edu
  • Phone: (507) 255-2440

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.