Evaluating Pacing Dependency After Aortic Valve Replacement

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on patients who have undergone transcatheter aortic valve replacement (TAVR) and subsequently received a permanent pacemaker. It aims to assess the prevalence of effective pacemaker stimulation one year after implantation, as well as three months post-procedure. The study will also analyze the types of conductive disorders associated with the need for pacing and the characteristics of patients who are or are not dependent on stimulation. The findings could provide insights into the long-term management of patients with high-grade conductive disorders following TAVR.

Why it matters

Who can join: the full rules

Inclusion Criteria:

all patients who need a permanent pacemaker implantation after TAVR

Exclusion Criteria:

Patients who have already a pace maker before TAVR

Where it's running

• University Hospital of Montpellier
  Montpellier, France Recruiting

Study contacts

• Study coordinator: Florence Leclercq, PUPH
• Email: f-leclercq@chu-montpellier.fr
• Phone: 0467336189

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.