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Clinical Trials/NCT05895097
NCT05895097
Not Yet Recruiting
N/A

Impact of Conduction System Pacing on Left Ventricular Remodeling After Transcatheter Aortic Valve Implantation

University Medical Centre Ljubljana1 site in 1 country50 target enrollmentJune 15, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aortic Valve Stenosis
Sponsor
University Medical Centre Ljubljana
Enrollment
50
Locations
1
Primary Endpoint
Left ventricular ejection fraction
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This randomized study compares the effects of conventional (right ventricular pacing in patients with LVEF ≥ 40% and cardiac resynchronization therapy in patients with LVEF < 40 %) versus left bundle branch pacing on left ventricular remodelling in patients with reduced left ventricular ejection fraction (< 50 %) that need permanent pacemaker implantation after transcatheter aortic valve implantation (TAVI).

Detailed Description

Bradycardic heart rhythm disturbances are a common complication of TAVI. Patients who will develop the indication for permanent pacemaker implantation after TAVI will be randomly assigned to either the experimental (left bundle branch pacing) or conventional (right ventricular pacing in patients with LVEF ≥ 40% and cardiac resynchronization therapy in patients with LVEF \< 40 %) group. The investigators will compare the left ventricular ejection fraction (primary outcome) 12 months after randomization. The investigators will also compare electrocardiographic (QRS duration), clinical (NYHA status, 6-minute walking test, handgrip test, Kansas City Cardiomyopathy Questionnaire) and laboratory (proBNP) parameters 6 and 12 months, and other echocardiographic (left ventricular systolic and diastolic diameter, signs of dyssynchrony, myocardial work) parameters 12 months after pacemaker implantation in both groups.

Registry
clinicaltrials.gov
Start Date
June 15, 2023
End Date
June 15, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Klemen Steblovnik

Principal Investigator

University Medical Centre Ljubljana

Eligibility Criteria

Inclusion Criteria

  • Indication for permanent pacemaker implantation after transcatheter aortic valve implantation (during the same hospitalization)
  • Left ventricular ejection fraction \< 50 %.

Exclusion Criteria

  • Unsuccessful TAVI procedure with life expectancy \< 1 year
  • Ischemic cardiomyopathy with interventricular septal fibrosis (at least echocardiographic signs of fibrosis)
  • Severe kidney failure (glomerular filtration rate \< 30 ml/min)
  • Previous permanent pacemaker

Outcomes

Primary Outcomes

Left ventricular ejection fraction

Time Frame: 12 months

Secondary Outcomes

  • NT-proBNP concentration(6 and 12 months)
  • NYHA status(6 and 12 months)
  • 6-minute walking test(6 and 12 months)
  • Hand grip test(6 and 12 months)
  • QRS duration(baseline, 6, and 12 months)
  • Left ventricular systolic diameter(12 months)
  • Left ventricular diastolic diameter(12 months)
  • Global constructive work(12 months)
  • Global work index(12 months)
  • Global wasted work(12 months)
  • Global work efficiency(12 months)
  • Signs of mechanical dyssynchrony(12 months)
  • Systolic pulmonary artery pressure (echocardiographic parameter)(12 months)
  • The Kansas City Cardiomyopathy Questionnaire (KCCQ-12)(6 and 12 months)

Study Sites (1)

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