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Actions Elicited by In-hospital Follow-up of Cardiac Devices

NCT01073449 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3362

Last updated 2011-02-28

Study results available
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Summary

This study will enroll all patients who will attend an in-hospital follow-up of cardiac device since February 22nd 2010 to June 21st 2010.

Primary objective of the study is to observe how many of patients seen during these period (approximately 5000) will receive a change in cardiac device programming or in drug therapy or a scheduled or urgent hospital admission.

These data should help to clarify how useful and safe is a remote monitoring strategy for this kind of patients.

Conditions

  • Cardiac Pacemaker, Artificial
  • Implantable Cardioverter-Defibrillator

Interventions

PROCEDURE

In-hospital follow-up of cardiac device

Electrical measures taken during normal follow-up and clinical status of the patient

Sponsors & Collaborators

  • Cliniche Humanitas Gavazzeni

    lead OTHER

Principal Investigators

  • Giosue Mascioli, MD · Cliniche Humanitas Gavazzeni

  • Antonio Curnis, MD · Spedali Civili di Brescia

  • Maurizio Landolina, MD · Policlinico San Matteo Pavia

  • Gian-Paolo Gelmini, MD · Ospedale Civile di Desenzano d/Garda

  • Franco Ruffa, MD · Ospedale A. Manzoni - Lecco

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01073449 on ClinicalTrials.gov