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A Registry Study to Assess SYNTHECELTM Dura Repair

NCT07758790 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 112

Last updated 2026-08-11

No results posted yet for this study

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.

Conditions

  • Craniotomy

Sponsors & Collaborators

  • DePuy Synthes Products, Inc.

    lead INDUSTRY

Principal Investigators

  • DePuy Synthes Product, Inc. Clinical Trial · DePuy Synthes Product, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2029-10-31
Completion
2030-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07758790 on ClinicalTrials.gov