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

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

Recruiting
18 years and older
All
Phase 4

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Overview

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.

Eligibility

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

Study details
    Wound Closure
    Brain Tumor Adult
    Spine
    Neurovascular
    Hemorrhagic Stroke
    Intracerebral
    Traumatic Brain Injury

NCT07225101

University of Michigan

1 February 2026

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