Medtronic PSR TDD PMCF
NCT04714385 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 209
Last updated 2024-06-04
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.
Conditions
- Chronic Pain
- Spasticity, Muscle
Sponsors & Collaborators
- lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-02-09
- Primary Completion
- 2024-01-18
- Completion
- 2024-01-18
Countries
- Belgium
- Czechia
- France
- Netherlands
- Slovenia
- Spain
- Switzerland
- United Kingdom
Study Locations
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