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PORTuguese Research on Telemonitoring With CareLink® (PORTLink)

NCT03125382 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 141

Last updated 2025-07-02

Study results available
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Summary

Compare use of Carelink system - monitoring system - with traditional in-clinic follow up, in patients with implantable cardiac defibrillator (ICD)

Conditions

Interventions

DEVICE

Carelink System

Patients start to perform device data transmission through Carelink system

DEVICE

In office standard visit

Patients start or maintain in office standard visits

Sponsors & Collaborators

  • Medtronic Cardiac Rhythm and Heart Failure

    lead INDUSTRY

Principal Investigators

  • Mário Oliveira, Doctor · Centro Hospitalar Lisboa Central

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2016-10-31
Completion
2016-10-31

Countries

  • Portugal

Study Locations

More Related Trials

Entities

Diseases

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 NCT03125382 on ClinicalTrials.gov