Tests a stitching device for closing wounds after brain and spine surgery
Tests the STRATAFIX suture in adults having brain or spine surgery.
Plain-language title generated from the registry record
Registry title: Evaluation of the Efficacy of STRATAFIX for Neurosurgical Cranial and Spine Procedures
Key facts
- Where
- Lansing, United StatesSee the site
- Phase
- Phase 4
Where in United States
- University of Michigan Health SparrowLansing, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University of Michigan
- Trial code
- NCT07225101
- Record updated
- 5 November 2025
- Original description
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.Read full original descriptionShow less
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.
Inclusion: Elective or emergent surgical approaches for cranial or spine neurosurgical approaches, requiring sutures for wound closure, requiring multilayer wound closure.
Exclusion: Patients with prior surgical wound dehiscence or infection; Patients with allergy to suture material.