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NCT05824676 · ClinicalTrials.gov registry record · NA
DePuy Synthes Variable Angle LCP Patella Plating System Study
A NA study, sponsored by Hartford Hospital.
- Not yet
- Registry status
- NA
- Development phase
- 36
- Enrollment target
NCT05824676 is a NA study that has not yet begun recruiting, run by Hartford Hospital. The registered enrollment target is 36 participants.
The verdict
NCT05824676, a NA study, has not yet begun recruiting, sponsored by Hartford Hospital.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
Study Summary
The Depuy Synthes Locking Compression Plate (LCP) Variable Angle Patella Plating System is an FDA approved device. The purpose of this study is to see how well the Depuy Synthes LCP Variable Plating System work in fixing a broken kneecap (patella). Depuy says that the device will improve healing when compared to traditional ways of repairing a broken patella. The goal of this randomized control trial is to learn how well the LCP Variable Plating System works to fix a broken patella (kneecap) compared to traditional fixation methods, in male and females, age 18 to 74, with a patellar fracture, and being treated at Hartford HealthCare The Bone and Joint Institute or Hartford Hospital. The main question it aims to answer are: * To understand if the Depuy Synthes LCP Variable Angle Plating System will provide a better way to help patients recover from a broken patella. Participants will evaluated at specific time points: post-op day 1, 6 weeks, 3 months, 6 months, and 12 month post-surgery. Participants will be asked to: * Complete surveys at all evaluation timepoints. * Have x-rays(radiographs) taken at the 6 week, 3 month, 6 month, 9 month, and 1 year timepoints. * Participants will have a passive range of motion tests done at 6 week, 3 month, 6 month, 9 month, and 1 year timepoints. * Participants would have strength and balance tests done at the 3 month, 6 month, 9 month, and 1 year timepoints.
Interventions
- DEVICE Variable Angle LCP Patella Plating System
- DEVICE Traditional Fixation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2023-05 |
| Est. Completion | 2027-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05824676
The ClinicalTrials.gov registry entry for NCT05824676 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hartford Hospital, which has 75 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Variable Angle LCP Patella Plating System is the first listed.
NCT05824676 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05824676 about?
NCT05824676 is a clinical study titled "DePuy Synthes Variable Angle LCP Patella Plating System Study". The Depuy Synthes Locking Compression Plate (LCP) Variable Angle Patella Plating System is an FDA approved device. The purpose of this study is to see how well the Depuy Synthes LCP Variable Plating System work in fixing a broken kneecap (patella). Depuy says that the device will improve healing whe...
What is the current status of trial NCT05824676?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 36 participants. The study started on 2023-05. Estimated completion is 2027-12.
What interventions are being tested in trial NCT05824676?
The interventions under investigation include: Variable Angle LCP Patella Plating System (DEVICE), Traditional Fixation (DEVICE).
Who is sponsoring clinical trial NCT05824676?
This trial is sponsored by Hartford Hospital, which has 75 total clinical trials registered on ClinicalTrials.gov.
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