Real Life Automatic Atrial Capture Device Control

NCT ID: NCT02400983

Last Updated: 2015-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

318 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-01-31

Study Completion Date

2015-03-31

Brief Summary

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The main objective of this study is to verify the effectiveness of the new ACAP ® Confirm algorithm in the automatic management of atrial capture.

Detailed Description

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Conditions

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Sinus Bradycardia Sinus Node Disease Atrio-ventricular Block Heart Failure

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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Pacemaker, ICD

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients had undergone first implantation or device replacement with a Medical device (PM, ICD, CRT-P, CRT-D) endowed with ACAP Confirm ® algorithm features between May 2011 and March 2012

Exclusion Criteria

* Atrial fibrillation
Minimum Eligible Age

18 Years

Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

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Maria Vittoria Hospital

OTHER

Sponsor Role lead

Responsible Party

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Dr.Massimo Giammaria

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Massimo Giammaria

Role: PRINCIPAL_INVESTIGATOR

Maria Vittoria Hospital

Other Identifiers

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01

Identifier Type: -

Identifier Source: org_study_id

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