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

RecruitingPhase 4

Sponsor: University of Michigan

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

Interventions: STRATAFIX PDS and Monocryl suture

Countries: United States

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 overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

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

Locations (1)

Lansing, Michigan, United States