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Right Ventricular Lead Placement in a Pacemaker Population: Evaluation of Apical and Alternative Position

NCT01647490 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 408

Last updated 2012-07-23

No results posted yet for this study

Summary

This study is a long-term, prospective, and controlled evaluation of the mechanical dyssynchrony induced by right ventricular apical pacing, both in acute (spontaneous and stimulated) and chronic (12 and 24 months); the study also evaluates the benefit of an alternative pacing site through measures of dyssynchrony in acute and chronic.

Conditions

  • Bradycardia
  • Heart Block
  • Sick Sinus Syndrome

Interventions

PROCEDURE

Permanent Cardiac Pacemaker Implantation

Sponsors & Collaborators

  • Ospedale Santa Maria di Loreto Mare

    lead OTHER

Principal Investigators

  • Carmine Muto, MD · Ospedale Santa Maria di Loreto Mare

  • Valeria Calvi, MD · Azienda Ospedaliero Universitaria "Vittorio Emanuele" - Ferrarotto

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2013-07-31
Completion
2015-07-31

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 NCT01647490 on ClinicalTrials.gov