Actively Recruiting
Acute Response to Left Bundle Branch Area Pacing With SyncAV
Led by Abbott Medical Devices · Updated on 2025-02-21
50
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical investigation is a prospective, single-arm, post-market, non-randomized, single-center study designed to evaluate the effectiveness of the SyncAV CRT dynamic atrioventricular (AV) delay feature when used with left bundle branch area pacing (LBBAP).
CONDITIONS
Official Title
Acute Response to Left Bundle Branch Area Pacing With SyncAV
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is 18 years of age and willing to comply with the study requirements
- Patients with approved indication for dual-chamber pacing or cardiac resynchronization therapy and scheduled to be implanted with an Abbott pacing system
- Patient has documented left bundle branch block (LBBB) or intraventricular conduction delay (IVCD)
- Patient has an intrinsic QRS duration 63 130 ms
- Patient has intact AV conduction with PR interval 64 250 ms
You will not qualify if you...
- Patient has a resting ventricular rate > 100 bpm
- Patient has AV Block (2nd or 3rd degree)
- Patient has documented persistent atrial tachycardia or atrial fibrillation
- Patient has had a recent myocardial infarction, ablation, electrolyte imbalance, or any condition within the last 90 days that would contraindicate pacing device programming changes in the opinion of the investigator
- Patient is currently participating in another clinical investigation
- Patient is pregnant or nursing
- Patient has other medical, anatomic, comorbid, social, or psychological conditions that could limit participation or compliance according to the investigator
- Patient does not have legal authority
- Patient is unable to read or write
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
I.R.C.C.S. Policlinico San Donato
San Donato Milanese, MI, Italy, 20097
Actively Recruiting
Research Team
N
Nima Badie, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here