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RECRUITING
NCT07225101
PHASE4

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

Sponsor: University of Michigan

View on ClinicalTrials.gov

Summary

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 Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2025-11-01

Completion Date

2026-12-31

Last Updated

2025-11-05

Healthy Volunteers

No

Interventions

DEVICE

STRATAFIX PDS and Monocryl suture

STRATAFIX, suture employs a novel incorporation of barbed components to suture resulting in tension holding closure with long-lasting absorbable suture.

Locations (1)

University of Michigan Health Sparrow

Lansing, Michigan, United States