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NCT07245810 · ClinicalTrials.gov registry record
Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up
A clinical trial of Mandibular Fractures and Orthognathic Surgical Procedures, sponsored by Stryker Craniomaxillofacial.
- Recruiting
- Registry status
- 80
- Enrollment target
- 2
- Study locations
NCT07245810: Recruiting study of Mandibular Fractures and Orthognathic Surgical Procedures, sponsored by Stryker Craniomaxillofacial.
NCT07245810 is a study of Mandibular Fractures and Orthognathic Surgical Procedures that is actively recruiting participants, run by Stryker Craniomaxillofacial. The registered enrollment target is 80 participants. The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07245810, a study of Mandibular Fractures and Orthognathic Surgical Procedures, is actively recruiting participants, sponsored by Stryker Craniomaxillofacial.
- RECRUITING
- Registry status
- 80 participants
- Enrollment target
- 2
- Study locations
Study Summary
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.
Primary Outcome
Assessed by reviewing adverse events in patient medical charts at time point after surgery. Used to document whether an unplanned revision surgery was required or not for patients.
Conditions Studied
Interventions
- DEVICE Orthognatic surgery, Reconstructive maxillofacial surgery, Mandible and maxillofacial trauma surgery
Study Locations (2)
New York
- New York Center for Orthognathic and Maxillofacial Surgery - New York
- New York Center for Orthognathic and Maxillofacial Surgery, Lake Success, New York - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2024-11-18 |
| Est. Completion | 2026-01-15 |
What NCT07245810 shows while recruiting
NCT07245810 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 80 participants, a relatively small participant target.
The record links to 4 conditions, with Mandibular Fractures appearing as the primary indexed condition, and to 1 intervention - of which Orthognatic surgery, Reconstructive maxillofacial surgery, Mandible and maxillofacial trauma surgery is the first listed.
NCT07245810 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT07245810 about?
NCT07245810 is a clinical study titled "Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up". 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.
What is the current status of trial NCT07245810?
This trial is currently recruiting. The enrollment target is 80 participants. The study started on 2024-11-18. Estimated completion is 2026-01-15.
What conditions does trial NCT07245810 study?
This clinical trial studies the following conditions: Mandibular Fractures, Orthognathic Surgical Procedures, Maxilla Fracture, Facial Fracture.
What interventions are being tested in trial NCT07245810?
The interventions under investigation include: Orthognatic surgery, Reconstructive maxillofacial surgery, Mandible and maxillofacial trauma surgery (DEVICE).
Who is sponsoring clinical trial NCT07245810?
This trial is sponsored by Stryker Craniomaxillofacial, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07245810 being conducted?
This trial has 2 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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