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SCANCAP Scandinavian Automatic Capture Study

NCT00180609 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 203

Last updated 2009-04-23

No results posted yet for this study

Summary

The primary objective of this study is to document the success rate of the automatic threshold testat pre-discharge in a normal pacemaker patient population implanted with Guidant Insignia Ultra or AVT .

Conditions

  • Bradycardia

Interventions

DEVICE

Automatic threshold test in Insignia Pacemakers from Guidant

Sponsors & Collaborators

  • Guidant Corporation

    lead INDUSTRY

Principal Investigators

  • Per D Christensen, MD · Medicinsk Afdeling, Sygehus Viborg, Viborg, Denmark

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-12-31
Completion
2006-07-31

Countries

  • Denmark

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 NCT00180609 on ClinicalTrials.gov