Real Life Automatic Atrial Capture Device Control

Maria Vittoria Hospital318 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

318

Conditions

Sinus Bradycardia Sinus Node Disease Atrio-ventricular Block Heart Failure

Interventions

Pacemaker, ICDDEVICE

Eligibility

Min age: 18 Years

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

The main objective of this study is to verify the effectiveness of the new ACAP Confirm ® algorithm in management of atrial capture in both new implants and patients undergoing device replacements with different manufactures atrial leads.

Time frame: 6 Months

Secondary Outcomes

Relationship with pulse width

Time frame: 6 Months

Clinical equivalence of automatic and manual thresholds tests results.

Time frame: 6 Months

Data from ClinicalTrials.gov

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