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APPROPRIATE - Rate Adaptive Pacing Sensor

NCT00757666 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 566

Last updated 2017-06-14

Study results available
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Summary

The APPROPRIATE study will compare differences in functional capacity (peak VO2) between chronotropically incompetent patients randomized to receive rate responsive pacing driven by either the minute ventilation (respiration-based) sensor or an accelerometer (motion-based).

Conditions

  • Heart Diseases

Interventions

DEVICE

Rate adaptive pacemaker

Accelerometer sensor

DEVICE

Rate adaptive pacemaker

Minute ventilation sensor

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Michael Giudici, MD · Genesis Heart Institute

  • F. Roosevelt Gilliam, MD · Cardiology Associates of NE Arkansas

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • United States

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 NCT00757666 on ClinicalTrials.gov