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

Recruiting now · Phase 4

Conditions studied: Wound Closure, Brain Tumor Adult, Spine, Neurovascular, Hemorrhagic Stroke, Intracerebral, Traumatic Brain Injury

In brief

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.

Key facts

Study ID

NCT07225101

Run by

University of Michigan

People needed

160

Starts

2025-11-01

Expected to finish

2026-12-31

Last updated by the study team

2025-11-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Elective or emergent surgical approaches for cranial or spine neurosurgical approaches, requiring sutures for wound closure, requiring multilayer wound closure

You may not qualify if…

• Patients with prior surgical wound dehiscence or infection
• Patients with allergy to suture material

Where it is running

• University of Michigan Health Sparrow — Lansing, Michigan, United States (enrolling)

Full record on ClinicalTrials.gov

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