Clinical Trials in the USA / NCT06822920
Recruiting
Observational
Post-Market Clinical Investigation Plan - Collagen Dura Membranes (DM & DMO)
NCT06822920 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Repair of Dura Mater
Study summary
Monitoring the Use of Collagen Dura Membrane in the Post-market phase
Eligibility
Inclusion Criteria:
* Patients with a dural defect requiring repair with a dural substitute.
Exclusion Criteria:
* There are no subject restrictions for the study other than patients with known allergy to bovine collagen products as specified in the contraindications of the Instructions for Use.
Primary outcome measure(s)
- Measurement of the occurrence of adverse event requiring surgical intervention — 6-9 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Medical Collagen of Wisconsin | Milwaukee | Wisconsin | Recruiting |
More Collagen Matrix trials in the USA
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06822920 on ClinicalTrials.gov ↗ ← All trials in the USA