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RECRUITING

Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow Up

NCT07245719 · View on ClinicalTrials.gov ↗

Study Summary

A retrospective post-market clinical follow-up to confirm the performance and safety of the Upper-Face and Mid-Face modules of the Stryker Universal CMF System in a clinical setting. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.

Interventions

  • DEVICE Upper-Face and/or Mid-Face modules (1.2 / 1.7 modules) of the Stryker Universal CMF System

Study Locations (1)

New York

  • Weill Cornell Medicine Oral and Maxillofacial Surgery 525 East 68th Street, F-2132 — New York

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-03-28
Est. Completion 2026-02

Sponsor

Stryker Craniomaxillofacial

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07245719

The ClinicalTrials.gov registry entry for NCT07245719 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stryker Craniomaxillofacial, which has 33 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Orbital Fractures appearing as the primary indexed condition, and to 1 intervention — of which Upper-Face and/or Mid-Face modules (1.2 / 1.7 modules) of the Stryker Universal CMF System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07245719 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07245719 about?

NCT07245719 is a clinical study titled "Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow Up". A retrospective post-market clinical follow-up to confirm the performance and safety of the Upper-Face and Mid-Face modules of the Stryker Universal CMF System in a clinical setting. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on ...

What is the current status of trial NCT07245719?

This trial is currently recruiting. The enrollment target is 120 participants. The study started on 2025-03-28. Estimated completion is 2026-02.

What conditions does trial NCT07245719 study?

This clinical trial studies the following conditions: Orbital Fractures, Zygomatic Fractures, Maxilla Fractures, Facial Fractures. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07245719?

The interventions under investigation include: Upper-Face and/or Mid-Face modules (1.2 / 1.7 modules) of the Stryker Universal CMF System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07245719?

This trial is sponsored by Stryker Craniomaxillofacial, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07245719 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial