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Procedure

LCP Patella Plating System vs Traditional Fixation for Knee Fracture

N/A
Waitlist Available
Research Sponsored by Hartford Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a special device for fixing broken kneecaps in adults aged 18-74. The device holds the broken pieces together securely, which may help them heal better than traditional methods.

Who is the study for?
This trial is for men and women aged 18-74 who have a broken kneecap and are being treated at Hartford HealthCare The Bone and Joint Institute or Hartford Hospital. It's not for those over 75, non-walkers before injury, with previous patellar fractures, knee arthritis, or other leg bone fractures.
What is being tested?
The study compares the DePuy Synthes LCP Variable Angle Patella Plating System to traditional methods of fixing a broken kneecap. Participants will be randomly assigned to one of the treatments and followed up with surveys, x-rays, range of motion tests, as well as strength and balance assessments over a year.
What are the potential side effects?
While specific side effects aren't listed here, typical risks may include pain at the fracture site, infection from surgery, issues with bone healing like nonunion or malunion (where bones don't heal properly), irritation from hardware placed in the knee.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
DePuy Synthes LCP Variable Angle Patella Plating System clinical outcomes comparison
DePuy Synthes LCP Variable Angle Patella Plating System functional outcomes comparison
DePuy Synthes LCP Variable Angle Patella Plating System patient reported outcomes comparison
Secondary study objectives
Activities of Daily Living-Knee Outcomes Survey (ADL-KOS)
Balance
Passive Range of Motion (ROM)
+3 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Depuy Synthes LCP Patella Plating SystemExperimental Treatment1 Intervention
This group will have 18 randomly selected participants, who will receive the Depuy Synthes LCP Patella Plating System for patella fracture.
Group II: Control/Conventional FixationExperimental Treatment1 Intervention
This group will have 18 randomly selected participants, who will receive the conventional treatment for patella fracture.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The Depuy Synthes Locking Compression Plate (LCP) Variable Angle Patella Plating System stabilizes knee fractures by allowing screws to be placed at variable angles, accommodating the unique anatomy of the patella and specific fracture patterns. This stability minimizes movement at the fracture site, reducing pain and promoting bone healing. The compression provided by the plate helps bring fractured bone fragments together, essential for proper healing. This method offers improved outcomes compared to traditional fixation methods, potentially leading to faster recovery and better healing.

Find a Location

Who is running the clinical trial?

Hartford HospitalLead Sponsor
138 Previous Clinical Trials
19,361 Total Patients Enrolled

Media Library

Traditional Fixation (Procedure) Clinical Trial Eligibility Overview. Trial Name: NCT05824676 — N/A
Knee Fracture Research Study Groups: Depuy Synthes LCP Patella Plating System, Control/Conventional Fixation
Knee Fracture Clinical Trial 2023: Traditional Fixation Highlights & Side Effects. Trial Name: NCT05824676 — N/A
Traditional Fixation (Procedure) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05824676 — N/A
~20 spots leftby Dec 2026