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DEtect Long-term Complications After icD rEplacement: a Multicenter Italian Registry

NCT02076789 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2015-01-09

No results posted yet for this study

Summary

This study has been designed to prospectively estimate long term complication rates (12-months and 5-years) in patients undergoing Implantable Cardioverter Defibrillator (ICD) replacement, with and without a planned transvenous lead addition for replacement or upgrade to a device capable of additional therapies; the study also evaluates the predictors of complications, the patient's management before and during the replacement procedure in clinical practice and the estimated costs related to the use of health care resources.

Conditions

  • Device Replacement
  • Device Upgrade
  • Long-term Postoperative Complications
  • Resource Consumption and Associated Costs After Device Replacement/Upgrade

Sponsors & Collaborators

  • Mauro Biffi

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2015-10-31
Completion
2015-10-31

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 NCT02076789 on ClinicalTrials.gov