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

Study acronym: UPC
StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 22, 2026 (before its estimated May 31, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Enrollment target: 80 to 726v2 Show 4 more changesShow less
    • Primary completion date: Nov 15, 2025 to May 31, 2026
    • Trial status: Recruiting to Active, Not Recruiting
    • Study completion date: Jan 15, 2026 to May 31, 2026
    • Site details revised at 2 of 2 sites
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07245810
Lead Sponsor Stryker Craniomaxillofacial
Conditions
(from sponsor)		 Mandibular Fractures, Facial Fracture, Maxilla Fracture, Orthognathic Surgical Procedures
Related terms Mandibular Fractures, Maxillary Fractures
Enrollment 726 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov