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Not Yet Recruiting
NCT07758790
A Registry Study to Assess SYNTHECELTM Dura Repair
Conditions: Craniotomy
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 112
Sponsor: DePuy Synthes Products, Inc.
Summary
The purpose of this study is to assess how safe synthecel dura repair is and how well it performs in participants undergoing cranial surgery requiring dura repair (a procedure to close and protect the outer covering of the brain) in a regular, everyday healthcare environment.
Eligibility Criteria
Inclusion Criteria:
* Participant or legally authorized representative who is willing to participate in the registry and provide written informed consent
* Participant undergoing SYNTHECEL implantation for cranial dura repair on or after the start date of the registry study
Exclusion Criteria:
\- Participant with documented or known hypersensitivity or allergic reaction to cellulose or related materials
Source: ClinicalTrials.gov (NCT07758790). StuddyBuddy aggregates publicly available trial information.
