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Evaluation of the Efficacy of STRATAFIX for Neurosurgical Cranial and Spine Procedures

RecruitingPhase 4Ages 18 Years - anyAllUniversity of Michigan
NCT07225101 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This research is studying a device already approved by the Food and Drug Administration (FDA) to treat wound closures. Researchers are studying a large group of people to continue to learn information about the safety of the STRATAFIX suture and how people's bodies react to using it over a long period of time. This research will provide additional information about using STRATAFIX sutures to close surgical wounds.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Elective or emergent surgical approaches for cranial or spine neurosurgical approaches, requiring sutures for wound closure, requiring multilayer wound closure Exclusion Criteria: * Patients with prior surgical wound dehiscence or infection * Patients with allergy to suture material
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What it tests

  • STRATAFIX PDS and Monocryl suture
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Where

1 site
University of Michigan Health Sparrow
Lansing, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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