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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01459874
Other study ID # HomeGuide
Secondary ID
Status Completed
Phase N/A
First received October 24, 2011
Last updated March 26, 2013
Start date March 2008
Est. completion date December 2011

Study information

Verified date March 2013
Source San Filippo Neri General Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics CommitteeItaly: National Institute of Health
Study type Observational

Clinical Trial Summary

The purpose of the registry is to evaluate an organizational model fixing roles and behaviors of subjects involved in the remote monitoring of patients implanted with pacemakers and defibrillators.

The evaluation will estimate the clinical efficiency and the impact on health service resources of the organizational model when this is implemented in the daily clinical practice.


Description:

After a number of studies which assessed technical reliability and clinical implications of remote monitoring systems, a further step should approach the issue of how remote monitoring can be implemented as a part of routine activities of a cardiology outpatient clinic. A clear definition of roles and workflow to timely manage information and properly react to adverse events is required. The HomeGuide Registry proposes an organizational model specifying roles and procedures for outpatient clinics using a specific remote monitoring system in routine follow-up. The HomeGuide model is essentially based on an interaction between one or more allied professionals (expert and trained nurses or technicians) and a responsible physician. The main objective of the HomeGuide Registry is to evaluate:

1. Clinical efficiency of remote patient management;

2. Health service resources required by a remote patient management.


Recruitment information / eligibility

Status Completed
Enrollment 1650
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients implanted with a BIOTRONIK pacemaker or ICD with Home Monitoring (HM) technology

- Ability to utilize the HM system throughout the study

- Ability to give informed consent

- Ability to return for regular follow-ups for two years

Exclusion Criteria:

- Patients who do not fulfill all inclusion criteria

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Implantable Cardioverter Defibrillator
  • Pacemaker

Intervention

Behavioral:
Organizational model for remote monitoring
An organizational model defining roles and behaviors of subjects involved in the remote monitoring of pacemaker and defibrillator recipients

Locations

Country Name City State
Italy Umberto I Hospital Altamura Bari
Italy G.M. Lancisi Hospital Ancona
Italy I.N.R.C.A. Ancona
Italy S. Donato di Arezzo Hospital Arezzo
Italy Presidio Ospedale di Ariano Irpino Ariano Irpino Avellino
Italy Policlinico - Card. Universitaria Bari
Italy Policlinico - Cardiologia Ospedaliera Bari
Italy Policlinico - Cardiologia Ospedaliera Benevento
Italy AO Spedali Civili Brescia
Italy Congreg. Ancelle della Carità Poliambulanza Brescia
Italy A. Perrino Hospital Brindisi
Italy Cardarelli Hospital Campobasso
Italy S. Cuore University Campobasso
Italy Carrara Civil Hospital Carrara
Italy PO Francesco Ferrari Casarano Lecce
Italy Sant'Anna e San Sebastiani Hospital Caserta
Italy San Leonardo Castellammare di Stabia Napoli
Italy Ferrarotto Hospital Catania
Italy ULSS n. 14 Chioggia Venezia
Italy Ulss n. 7 Conegliano Treviso
Italy Ospedale di Circolo Desio Monza e Brianza
Italy AO Arcispedale S. Anna Ferrara
Italy A.O.U. Careggi S.O.D. Aritmologia Firenze
Italy S. Giovanni di Dio Hospital Firenze
Italy S. Maria Annunziata Hospital Firenze
Italy S. Maria Nuova Hospital Firenze
Italy P.O. Di Gorizia Gorizia
Italy F. Veneziale Hospital Isernia
Italy Vito Fazzi Hospital Lecce
Italy Mater Salutis Hospital Legnago Verona
Italy P.O. Giannuzzi Manduria Taranto
Italy Paolo Borsellino Hospital Marsala Trapani
Italy P. O. Villa D'Agri Marsicovetere Potenza
Italy Piemonte Hospital Messina
Italy Dell'Angelo Hospital Mestre Venezia
Italy Sacco Hospital Milano
Italy P.O.G. Fogliani Milazzo Messina
Italy Mirano Hospital Mirano Venezia
Italy Montebelluna Hospital Montebelluna Treviso
Italy F.B.F. Napoli
Italy Federico II Hospital Napoli
Italy Monaldi Hospital - Gruppo Sun Napoli
Italy Monaldi Hospital, U.O. Aritmologia Napoli
Italy Policlinico Federico II Napoli
Italy G. B. Grassi Ostia Roma
Italy Policlinico Universitario di Padova Padova
Italy ARNAS Civico Palermo
Italy Cervello Hospital Palermo
Italy Santa Maria della Misericordia Hospital Perugia
Italy SS. Cosimo e Damiano Hospital Pescia Pistoia
Italy Guglielmo da Saliceto Civil Hospital Piacenza
Italy Santa Maria degli Angeli Hospital Pordenone
Italy Portogruaro Hospital Portogruaro Venezia
Italy Santa Maria Nuova Hospital Reggio Emilia
Italy Degli Infermi Hospital Rimini
Italy Casa di Cura Villa Pia Roma
Italy Policlinico Casilino Roma
Italy Policlinico Tor Vergata Roma
Italy Policlinico Umberto I Roma
Italy San Filippo Neri Hospital Rome
Italy San Giovanni di Dio e Ruggi D'Aragona Hospital Salerno
Italy San Donà di Piave Hospital San Donà di Piave
Italy Teresa Masselli Mascia Hospital San Severo
Italy Senigallia Civil Hospital Senigallia Ancona
Italy Santa Maria Della Misericordia Hospital Sorrento Salerno
Italy P.O. SS. Annunziata Taranto
Italy Michele Sarcone Hospital Terlizzi Bari
Italy Sant'Antonio Abate Hospital Trapani
Italy Ca' Foncello Hospital Treviso
Italy Di Circolo Hospital Varese
Italy Macchi Hospital Varese
Italy SS. Giovanni e Paolo Hospital Venezia
Italy Guizzardi Hospital Vittoria Ragusa
Italy Volterra Hospital Volterra Pisa

Sponsors (2)

Lead Sponsor Collaborator
San Filippo Neri General Hospital Biotronik Italia

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Ricci RP, Morichelli L, D'Onofrio A, Calò L, Vaccari D, Zanotto G, Curnis A, Buja G, Rovai N, Gargaro A. Effectiveness of remote monitoring of CIEDs in detection and treatment of clinical and device-related cardiovascular events in daily practice: the Hom — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity, positive predictive value and expected utility of the organizational model Sensitivity, positive predictive value and expected utility in the detection of all cardiovascular and device-related events of the proposed organizational model Up to two years No
Secondary Manpower of the organizational model Health care source consumption required to implement the organizational model for the remote management of patients Up to two years No
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