Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up

Running, not enrolling

Conditions studied: Mandibular Fractures, Facial Fracture, Maxilla Fracture, Orthognathic Surgical Procedures

In brief

A retrospective post market follow up to confirm safety and performance of Stryker's Facial iD Universal Plate Configurator (UPC) implants in the clinical setting. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.

Key facts

Study ID

NCT07245810

Run by

Stryker Craniomaxillofacial

People needed

726

Starts

2024-11-18

Expected to finish

2026-05-31

Last updated by the study team

2026-04-22

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who received a Stryker UPC plate for osteotomy, stabilization and rigid fixation of maxillofacial fractures or reconstruction as per routine clinical practice
• Patients for whom data on the primary outcome variable is available.

You may not qualify if…

• Patients with non-reducible and unstable fractures at the time of surgery
• Patients with fractures of a severely atrophic mandible at the time of surgery
• Patients with active local infections at the time of surgery
• Patients with metal allergies and/or foreign body sensitivity at the time of surgery
• Patients with limited blood supply or insufficient quality or quantity of bone at the time of surgery
• Potentially non-compliant patients who are unwilling or incapable of following postoperative care instructions

Where it is running

• New York Center for Orthognathic and Maxillofacial Surgery — New York, New York, United States
• New York Center for Orthognathic and Maxillofacial Surgery, Lake Success, New York — New York, New York, United States

Full record on ClinicalTrials.gov

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