PANORAMA Observational Study

NCT00382525 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8586

Last updated 2025-07-03

No results posted yet for this study

Summary

To construct a computerized database of national profiles and epidemiological data on patients wearing Medtronic implantable pacemakers and cardioverter defibrillators (both with or without cardiac resynchronization therapy), implantable loop recorders and leads used within their intended use.

Clinical variables will be analyzed in relation to device-based data and diagnostics.

Conditions

Interventions

DEVICE

Cardiac Rhythm Management device

Sponsors & Collaborators

  • Medtronic Cardiac Rhythm and Heart Failure

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-31
Primary Completion
2012-10-31
Completion
2013-03-31

Countries

  • Belgium
  • India
  • Kuwait
  • Russia
  • Saudi Arabia
  • Serbia and Montenegro

Study Locations

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Entities

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 NCT00382525 on ClinicalTrials.gov