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Medtronic PSR TDD PMCF

OverviewStructured DataIssuesContributors

Contents

clinicaltrials.gov/study/NCT04714385
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT047143850
Health Conditions in Trial
‌
Chronic pain
0
Trial Recruitment Size
2090
Trial Sponsor
Medtronic
Medtronic
0
Clinical Trial Start Date
February 9, 2017
0
Primary Completion Date
December 30, 2023
0
Study Completion Date
December 30, 2023
0
Clinical Trial Study Type
Observational0
Observational Clinical Trial Type
Cohort0
Observational Study Perspective
Prospective0
Participating Facility
Maastricht
Maastricht
0
Madrid
Madrid
0
Marseille
Marseille
0
‌
Nottwil
0
Wilrijk
Wilrijk
0
Morges
Morges
0
Middlesbrough
Middlesbrough
0
Sint-Niklaas
Sint-Niklaas
0
...
Official Name
Product Surveillance Registry (PSR) - Targeted Drug Delivery (TDD) - SynchroMed II European Post-Market Clinical Follow-up (PMCF)0
Last Updated
November 1, 2023
0
Study summary

The purpose of this study is to provide continuing evaluation and reporting of safety and performance of the SynchroMed II Infusion System within its intended use. Data will support post-market surveillance obligations.

Timeline

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References

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