LIFE Study - Limiting Chronotropic Incompetence for Pacemaker Recipients

NCT00146861 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2017-05-18

No results posted yet for this study

Summary

This study will compare how two different sensors inside the pacemaker may affect patients' quality of life.

Conditions

  • Bradycardia

Interventions

DEVICE

sensor programming

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • James Coman, MD · Oklahoma Heart Institute

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-31
Primary Completion
2006-01-31
Completion
2006-01-31

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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 NCT00146861 on ClinicalTrials.gov