Suturable DuraGen™ PMCF Study

Status Active, not recruiting

Clinical Trial Summary

The primary goal of this study is to retrospectively collect data on the safety and efficacy of Suturable DuraGen™.

Clinical Trial Description

This is a multicenter, non-randomized, non-interventional, retrospective Post-Market Clinical Follow-up (PMCF) study to evaluate the occurrence of post-operative cerebrospinal fluid (CSF) leaks within 30 days (and up to 90 days) after use of Suturable DuraGen™ for a supratentorial, infratentorial, or spinal procedure. ;

Study Design

Related Conditions & MeSH terms

Cerebrospinal Fluid Leak

Clinical Trial Details

NCT number	NCT04923867
Study type	Observational
Source	Integra LifeSciences Corporation
Contact
Status	Active, not recruiting
Phase
Start date	April 28, 2021
Completion date	December 31, 2024

View Details

See also
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