CompletedNot Applicable

Electrophysiologic HV-interval as a Predicor for Permanent Pacemaker Implantation After TAVI

Germany25 participantsStarted 2012-12

Plain-language summary

The development of a high grade AV-block is a frequent complication associated with transcatheter aortic valve implantation (TAVI). Patients who were suitable for TAVI will be enrolled in this study. The HV-interval will be determined before and immediately after implantation. The hypothesis is that a prolonged HV-interval is associated with a high rate of complete AV-block following TAVI.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * symptomatic aortic valve stenosis * patients screened for TAVI * written informed consent Exclusion Criteria: * unconsciousness, not able to consent * \< 18 years * permanent pacemaker

What they're measuring

Determination of HV interval

Timeframe: Changes in Baseline to 24 hours

Trial details

NCT IDNCT01801098

SponsorKlinik für Kardiologie, Pneumologie und Angiologie

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2013-11

View on ClinicalTrials.gov More Symptomatic Aortic Valve Stenosis trials