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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | October 2016 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | December 24, 2025 |
| Trial ID | NCT03008291 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.
-
Personalized pacemaker rate setting to improve symptoms in heart failure with bradycardia
Researchers will try adjusting the pacemaker lower rate to a personalized, hemodynamically optimized heart rate to see if it reduces symptoms in people with heart failure who need a pacemaker.
-
BIOTRONIK CSP Lead Registry for Left Bundle Branch Area Pacing
This registry tests BIOTRONIK’s CSP-based pacing lead in patients needing a pacemaker or CRT, to see how it performs in real-life use.
-
Left bundle branch area pacing with Tendril STS or UltiPace leads
This study will try left bundle branch area pacing with the Tendril STS or UltiPace lead in adults who need pacemaker leads for bradycardia or related heart conditions to see if pacing and sensing are safe and work through six months after implant.
-
Using Apple Watch data to predict heart failure outcomes
This study is testing if data from Apple Watches can help predict heart failure problems and the chances of needing to go back to the hospital for patients with heart failure.
-
Ultra-high-frequency ECG to diagnose ventricular electrical dyssynchrony in patients getting pacemakers
This test checks whether an ultra-high-frequency ECG can safely and accurately detect ventricular dyssynchrony in adults with bradycardia or heart failure who are having their first pacemaker implanted.
-
Comparing Aortix Device to Diuretics for Acute Heart Failure
This study is testing whether the Aortix device can help people with acute heart failure who aren't responding to diuretics feel better compared to standard treatment.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.