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NCT06436053Recruiting

Acute Response to Left Bundle Branch Area Pacing With SyncAV

Source: ClinicalTrials.gov · Last updated 9 Jul 2026

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
24 May 2024
Start date
15 May 2024
Primary completion date
15 Dec 2026
Lead sponsor
Abbott Medical Devices
NCT number
NCT06436053

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 15 May 2024 to the primary completion date, 15 Dec 2026
  • 1 site 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.

Other illness

  • Patient has had a recent myocardial infarction, ablation, electrolyte imbalance, or any condition within the last 90 days that would contraindicate for pacing device programming changes in the opinion of the investigator
  • Patient has other medical, anatomic, comorbid, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements, or impact the scientific soundness of the clinical investigation results

Other

  • 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 is currently participating in another clinical investigation
  • Patient is pregnant or nursing
  • Patient does not have legal authority
  • Patient is unable to read or write

Who the study is looking for

  • 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 ≥ 130 ms
  • Patient has intact AV conduction with PR interval ≤ 250 ms

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
I.R.C.C.S. Policlinico San Donato
Coordinator of this site? Confirm its status
San Donato MilaneseItalyRecruiting

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