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Clinical Trial Summary

Post-Market Clinical Follow-up Registry of Patients with CODMAN CERTAS Plus Programmable Valves.


Clinical Trial Description

The CODMAN CERTAS Plus Programmable Valve is a single use implantable device designed for shunting cerebrospinal fluid (CSF) for the treatment of hydrocephalus. The valve can be set to 8 different performance settings for intraventricular pressure and drainage of CSF. The performance setting of the valve can be set preoperatively and can also be noninvasively changed post-implantation. This clinical investigation will maintain data for each patient from the date of implant through 3 years post-implantation. Data collection for each patient will occur per standard of care. However, the clinical investigation specifically aims to collect and analyze data from the day of procedure, and post-operatively at 1 month, 3 months, 6 months, 12 months, 24 months, and 36 months. Data from follow-up visits will be analyzed according to pre-defined time-intervals referring to these follow-up moments. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05397106
Study type Observational
Source Integra LifeSciences Corporation
Contact Maria Salmon-Sargeant
Phone 339-206-2979
Email maria.salmonsargeant@integralife.com
Status Recruiting
Phase
Start date January 24, 2023
Completion date September 30, 2027

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