Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086
NCT ID: NCT01522755
Last Updated: 2025-07-02
Study Results
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View full resultsBasic Information
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COMPLETED
409 participants
OBSERVATIONAL
2011-05-31
2013-12-31
Brief Summary
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Success of a pacing lead implant can be defined considering 3 items: ease of lead implant, lead stability and lead electrical performances.
These factors may be related to the physician experience (global implant experience, experience with a given lead), to the implant procedure (lead access, lead position, implant time, scopy time) to the lead (handling and mechanical characteristics) and to the patient (ischemic history).
Even though implant success rate is quite high with currently available leads, the weight of the different factors influencing success has never been studied systematically. The objective of the current study is then to define the predictive factors of an implant success with the CapsureFix MRI model 5086.
This lead has been selected because it has been available for a short period, so the investigators have a limited experience of it and it has a unique design which makes it conditionally safe in an MRI environment and which may be associated with specific handling characteristics.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients implanted with the CapsureFix MRI pacing lead
Patients implanted with the CapsureFix MRI pacing lead model 5086
Pacing system implant with the CapsureFix MRI pacing lead model 5086
Pacing system implant with the CapsureFix MRI pacing lead model 5086
Interventions
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Pacing system implant with the CapsureFix MRI pacing lead model 5086
Pacing system implant with the CapsureFix MRI pacing lead model 5086
Eligibility Criteria
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Inclusion Criteria
* Patient implanted with a fully automatic ICD and remotely followed-up,
* Patient geographically stable and able to attend FU at investigative site
* Patient who signed a data release authorization form,
Exclusion Criteria
* Patient already enrolled in a clinical study whose procedures may interfere with the results of the present study,
* Patients in New York Heart Association (NYHA) class IV
18 Years
ALL
No
Sponsors
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Medtronic
INDUSTRY
Medtronic Cardiac Rhythm and Heart Failure
INDUSTRY
Responsible Party
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Principal Investigators
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Olivier BIZEAU, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Regionnal d'Orléans La Source
Locations
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Centre Hospitalier Regionnal d'Orléans La Source
Orléans, , France
Countries
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Other Identifiers
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11
Identifier Type: -
Identifier Source: org_study_id
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