RECRUITING

Product Surveillance Registry

Description

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

Conditions

Cardiac Rhythm DisordersUrological DisordersNeurological DisordersCardiovascular DisordersDigestive DisordersIntracranial AneurysmMechanical Circulatory SupportRespiratory TherapyAortic, Peripheral Vascular and Venous DisordersMinimally Invasive Surgical ProceduresDiagnostic Techniques and ProceduresSurgical Procedures, OperativeRenal InsufficiencyNeurovascularCoronary Artery DiseaseEar, Nose and Throat Disorder
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Related Conditions:

Cardiac Rhythm DisordersUrological DisordersNeurological DisordersCardiovascular DisordersDigestive DisordersIntracranial AneurysmMechanical Circulatory SupportRespiratory TherapyAortic, Peripheral Vascular and Venous DisordersMinimally Invasive Surgical ProceduresDiagnostic Techniques and ProceduresSurgical Procedures, OperativeRenal InsufficiencyNeurovascularCoronary Artery DiseaseEar, Nose and Throat Disorder

Study Overview

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Study Details

Study overview

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

Medtronic Product Surveillance Registry

Product Surveillance Registry

Condition
Cardiac Rhythm Disorders
Intervention / Treatment

-

Contacts and Locations

Birmingham

Birmingham, Alabama, United States,

Huntsville

Huntsville, Alabama, United States,

Anchorage

Anchorage, Alaska, United States,

Chandler

Chandler, Arizona, United States,

Phoenix

Phoenix, Arizona, United States,

Jonesboro

Jonesboro, Arkansas, United States,

Little Rock

Little Rock, Arkansas, United States,

Aliso Viejo

Aliso Viejo, California, United States,

Carlsbad

Carlsbad, California, United States,

Chula Vista

Chula Vista, California, United States,

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
  • * Patient has or is intended to receive or be treated with an eligible Medtronic product
  • * Patient within enrollment window relative to therapy initiation or meets criteria for retrospective enrollment
  • * Patient who is, or will be, inaccessible for follow-up
  • * Patient with exclusion criteria required by local law
  • * Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Medtronic,

Study Record Dates

2030-01