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NCT06105580Recruiting

Conduction System Pacing vs Biventricular Pacing in Systolic Dysfunction and Wide QRS: Mortality, Heart Failure Hospitalization or Cardiac Transplant

Conduction System Pacing vs Biventricular Resynchronization Therapy in Systolic Dysfunction and Wide QRS: Mortality, Heart Failure Hospitalization or Cardiac Transplant

Source: ClinicalTrials.gov · Last updated 3 Apr 2026

Brief summary (registry, in English)

Conduction system pacing vs biventricular resynchronization therapy in systolic dysfunction and wide QRS: mortality, heart failure hospitalization or cardiac transplant (CONSYST-CRT II trial). Superiority trial that aims to study the composite endpoint consisting of all-cause mortality, cardiac transplant or heart failure hospitalization at 12-month follow-up.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
320 (estimated)
First submitted
4 Oct 2023
Start date
27 Nov 2023
Primary completion date
Nov 2027
Lead sponsor
Hospital Clinic of Barcelona
NCT number
NCT06105580

What you commit to

  • Study type: Interventional
  • Planned participants: 320
  • From 27 Nov 2023 to the primary completion date, Nov 2027
  • 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.

Prior treatment

  • Myocardial infarction, unstable angina or cardiac revascularization during the previous 3 months.

Other

  • Pregnancy.
  • Participating currently in a clinical investigation that includes an active treatment.

Who the study is looking for

  • Patient must indicate acceptance to participate in the study by signing an informed consent document.
  • Patient must be ≥ 18 years of age.
  • Left bundle branch block, QRS ≥130 and LVEF \<=35%. No indication of stimulation for AV block.
  • Non-left bundle branch block, QRS ≥150 and LVEF \<=35%.
  • Resynchronization therapy indication for ventricular dysfunction (LVEF \<40%) and indication of cardiac pacing for AV block.
  • LVEF \<=35% in NYHA class III or IV, atrial fibrillation and intrinsic QRS \>=130 ms, provided a strategy to ensure biventricular capture is in place.

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hospital Clinic de Barcelona
Coordinator of this site? Confirm its status
BarcelonaSpainRecruiting

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