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NCT07492979Recruiting

Conduction System Pacing vs. Biventricular Pacing for Cardiac Resynchronization Therapy

Nordic-CSP - a Randomized Nordic Study - Is Conduction System Pacing Superior Compared to Conventional BIV-CRT in Reducing the Death or Heart Failure-related Hospitalization in Patients With Heart Failure and Bundle Branch Block?

Source: ClinicalTrials.gov · Last updated 28 Jul 2026

Brief summary (registry, in English)

The NORDIC-CSP trial is an investigator-initiated, blinded, nordic RCT aimed at evaluating whether using direct pacing of the HIS bundle (HIS)-pacing or left bundle branch (LBB) pacing is superior to conventional biventricular pacing in reducing the incidence of the composite endpoint of death and non-planned HF hospitalization. The study will be conducted in the 4 CRT-centres in Denmark and 6-8 centres from countries Sweden, Norway and Finland.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
1100 (estimated)
First submitted
10 Feb 2026
Start date
Jun 2026
Primary completion date
Mar 2031
Lead sponsor
Copenhagen University Hospital, Rigshospitalet
NCT number
NCT07492979

What you commit to

  • Study type: Interventional
  • Planned participants: 1100
  • From Jun 2026 to the primary completion date, Mar 2031
  • 5 sites in 4 countries
  • 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

  • treatment with a cardiac implantable electronic device (CIED) is contraindicated.

Other illness

  • recent acute myocardial infarction (AMI)

Lab values

  • Patients are excluded with regards to the MRI sub study if eGFR \> 35 ml/min, in case or contrast allergy or certain metal implants.

Age

  • life expectancy \<2 years, patients in hemodialysis

Other

  • coronary artery bypass graft (CABG) (\<3 months)

Who the study is looking for

  • ≥18 years of age,
  • LVEF ≤ 35%,
  • NYHA Class II-IV (IV only outpatients),
  • optimized in medical treatment (OMT)
    • AND one of the following:
    • . LBBB according to AHA/ACC/HRS Scientific Statement from 2009 and ≥130ms or
  • LBBB-like intraventricular conduction delay (IVCD) \> 150ms or RV paced QRS and indication for upgrade to CRT (\> 40% RV pacing) OR
  • ≥18 years of age,
  • LVEF ≤ 40 %
  • pacing indicated by AV-block and, thus, expected large percentage of ventricular pacing.

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

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

SiteCityCountrySite status
Dept. of Cardiology, Aarhus University Hospital, Aarhus
Coordinator of this site? Confirm its status
AarhusDenmarkNot yet recruiting
Rigshospitalet (Copenhagen University Hospital)
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting
Dept of Cardiology, Meilahti Hospital, Helsinki
Coordinator of this site? Confirm its status
HelsinkiFinlandNot yet recruiting
Haukeland Universitetssykehus
Coordinator of this site? Confirm its status
BergenNorwayNot yet recruiting
Sahlgrenska University Hospital
Coordinator of this site? Confirm its status
GothenburgSwedenNot yet recruiting

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