Assessment of the Performance of LYoplant® ONlay for Duraplasty
NCT02678156 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 61
Last updated 2025-04-16
Summary
The aim of this Post Market Clinical Follow-up Study is to collect clinical data on the performance of Lyoplant® Onlay. To assess the performance of the product, various safety and efficacy parameters have been selected.
Conditions
- Craniotomy
- Duraplasty
- Spinal Surgery
Interventions
- DEVICE
-
Lyoplant Onlay
Sponsors & Collaborators
-
Aesculap AG
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-04-30
- Primary Completion
- 2017-10-31
- Completion
- 2018-02-19
Countries
- Germany
Study Locations
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