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Search / Trial NCT02482844

Assessment of the Prognosis of Persistent Left Bundle Branch Block (LBBB)After Transcatheter Aortic Valve Implantation (TAVI ) by an Electrophysiological and Remote Monitoring Risk-adapted Algorithm

Launched by UNIVERSITY HOSPITAL, CLERMONT-FERRAND · Jun 25, 2015

Trial Information

Current as of July 21, 2025

Unknown status

Keywords

Tavi De Novo And Persistent Lbbb Electrophysiology Holter Pacemaker

ClinConnect Summary

The aim of this protocol is to study the appearance of the high grade AV conductive disorders at 12 months by monitoring for patients with a de novo LBBB after TAVI from an adapated algorithm to the risk and based on an early electrophysiological evaluation.

The recruitment of patients takes place in each cardiology department. The project is submitted to the Ethics Committee .

The patients are informed about this study by the investigator. After a reflection period and an answer to the possible questions, the patient is included. The informed consent is signed.

Every patient included wi...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients over 18 year's old
  • Patient implanted by a percutaneous biological aortic valve according to the recommendations of the European society of cardiology according to the guidelines of ESC 2012
  • Life expectancy upper 1-year-old
  • Sinusal rhythm
  • Patient with a de novo LBBB post-TAVI persitent and observed beyond 24 hours after the procedure of TAVI.
  • Exclusion Criteria:
  • Patient with a pacemaker pre-TAVI
  • Patient with LBBB pre-procedure
  • Pregnancy
  • Permanent atrial fibrillation

About University Hospital, Clermont Ferrand

The University Hospital of Clermont-Ferrand is a leading academic medical institution dedicated to advancing healthcare through innovative research and clinical trials. Renowned for its multidisciplinary approach, the hospital integrates cutting-edge scientific inquiry with patient care, fostering an environment that promotes collaboration among healthcare professionals, researchers, and academic partners. With a strong commitment to improving patient outcomes, the institution actively engages in a wide array of clinical studies, ranging from early-phase trials to large-scale interventions, aimed at addressing critical health challenges and enhancing treatment modalities. Its state-of-the-art facilities and expertise make it a pivotal contributor to clinical research in the region and beyond.

Locations

Clermont Ferrand, , France

Patients applied

0 patients applied

Trial Officials

Romain ESCHALIER

Principal Investigator

University Hospital, Clermont-Ferrand

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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