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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: Clinical Trial NA study, sponsored by Hartford Hospital.
NCT05824676 is a NA study that has not yet begun recruiting, run by Hartford Hospital. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Comparing the DePuy Synthes LCP Variable Patella Plating System to tradition fixation methods using clinical outcomes measures.
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 |
What is known before NCT05824676 opens enrollment
NCT05824676 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which Variable Angle LCP Patella Plating System is the first listed.
NCT05824676 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05824676's enrollment target sits among peer trials
36 1541st of 2000 higher than 437 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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