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NCT07221916 · ClinicalTrials.gov registry record
Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up
A clinical trial of Mandibular Reconstruction and Mandible Fracture, sponsored by Stryker Craniomaxillofacial.
- Recruiting
- Registry status
- 50
- Enrollment target
- 2
- Study locations
NCT07221916: Recruiting study of Mandibular Reconstruction and Mandible Fracture, sponsored by Stryker Craniomaxillofacial.
NCT07221916 is a study of Mandibular Reconstruction and Mandible Fracture that is actively recruiting participants, run by Stryker Craniomaxillofacial. The registered enrollment target is 50 participants. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07221916, a study of Mandibular Reconstruction and Mandible Fracture, is actively recruiting participants, sponsored by Stryker Craniomaxillofacial.
- RECRUITING
- Registry status
- 50 participants
- Enrollment target
- 2
- Study locations
Study Summary
A retrospective post market follow up to confirm safety and performance of Stryker's Surgeon iD Plates (SMRP) medical device. The study is performed to confirm the product's performance and safety by systematically collecting clinical data on its use.
Primary Outcome
Rate of unplanned revision surgery determined by reviewing adverse events in patient medical charts after surgery. Used to document whether an unplanned revision surgery was required or not for each patient.
Conditions Studied
Interventions
- DEVICE Mandibular Reconstruction
Study Locations (2)
California
- UCSF Otolaryngology Head and Neck Surgery - San Francisco
Other
- Heinrich-Braun-Klinikum gGmbH - Zwickau
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-12-01 |
| Est. Completion | 2025-12-31 |
What NCT07221916 shows while recruiting
NCT07221916 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target.
The record links to 2 conditions, with Mandibular Reconstruction appearing as the primary indexed condition, and to 1 intervention - of which Mandibular Reconstruction is the first listed.
NCT07221916 reports a single indexed study location in California, Other.
Frequently Asked Questions
What is clinical trial NCT07221916 about?
NCT07221916 is a clinical study titled "Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow Up". A retrospective post market follow up to confirm safety and performance of Stryker's Surgeon iD Plates (SMRP) medical device. 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 NCT07221916?
This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2024-12-01. Estimated completion is 2025-12-31.
What conditions does trial NCT07221916 study?
This clinical trial studies the following conditions: Mandibular Reconstruction, Mandible Fracture.
What interventions are being tested in trial NCT07221916?
The interventions under investigation include: Mandibular Reconstruction (DEVICE).
Who is sponsoring clinical trial NCT07221916?
This trial is sponsored by Stryker Craniomaxillofacial, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07221916 being conducted?
This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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