Clinical Trials in the USA / NCT07371091
Starting soon
Observational
Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - Repair (DMR)
NCT07371091 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Repair of Dura Mater
Study summary
Monitoring the Use of Collagen Dura Regeneration Membrane - Repair (DMR) in the Post-market Phase.
Eligibility
Inclusion Criteria:
* Patients with a dural defect requiring repair with a dural substitute as per routine clinical practice
* Patient is 18 years or older
* Patient of child-bearing potential is not pregnant or nursing
* Participant is willing and able to provide consent
Exclusion Criteria:
* Patients with a known history of hypersensitivity to bovine derived materials
* Patients that are non-English speaking
* Patients requiring legal representation
Primary outcome measure(s)
- Rate of Revision Surgery — at least one timepoint at 8 months or more post-surgery
Rate of adverse events related to the Subject Device requiring surgical intervention.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Rush University Medical Center | Chicago | Illinois | |
| Massachusetts General Hospital | Boston | Massachusetts |
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 NCT07371091 on ClinicalTrials.gov ↗ ← All trials in the USA