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

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.

Trial Details

NCT ID

NCT07225101

Phase

PHASE4

Sponsor

University of Michigan

Status

RECRUITING

Cancer Type

Brain Cancer

Interventions

STRATAFIX PDS and Monocryl suture

Locations (sample)

Lansing, Michigan, United States|42.73253,-84.55553

Key Eligibility Criteria

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

For full eligibility, visit ClinicalTrials.gov.

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