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OpenTrials
Completed

NCT Number: NCT00701467

Change in Heart Rate Variability Prior to Tachyarrhythmia in ICD Implanted Patients

To investigate changes in HRV during the time before a spontaneous episode of ventricular tachyarrhythmia.

Completed

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • S/P lexos VR/-T,DR/-T implantation
  • Signed patient informed consent

Exclusion criteria

  • CAF
  • Life expectancy<6 months
  • Impending heart transplant
  • Persistent recurring tachycardia
  • Rhythm disturbances that preclude a meaningful HRV analysis
  • Participation in another study.

Treatment and study plan

Primary outcomes

  1. Change in RR interval recorded by ICD

    Time frame: within an hour before ventricular tachyarrythmia

Sponsors and collaborators

Lead sponsor

Sheba Medical Center

Other Gov

Registry information

Official study title

HRV Registry to Investigate Changes During the Time Before a Spontaneous Episode of Ventricular Tachyarrhythmia

Acronym: HRV

Important dates

Study start
2008
Primary completion
2010
Study completion
2013
First posted
Jun 19, 2008
Registry last updated
Nov 19, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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