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NCT07280169 · ClinicalTrials.gov registry record · NA

Carbo-fix Lateral Plate Devices and Standard Plate-Nail Constructs in Distal Femur Fractures

A NA study of Distal Femur Fracture, sponsored by University of Missouri-Columbia.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT07280169 is a NA study of Distal Femur Fracture that is actively recruiting participants, run by University of Missouri-Columbia. The registered enrollment target is 100 participants, below the 133-participant average among 4 other Distal Femur Fracture trials with a reported enrollment target (25% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07280169, a NA study of Distal Femur Fracture, is actively recruiting participants, sponsored by University of Missouri-Columbia.

RECRUITING
Registry status
NA
Development phase
100 participants
Enrollment target
1
Study location

Study Summary

The purpose of this randomized clinical trial is to decrease non-union rates in distal femur fracture fixation. Carbo-fix lateral femur plate and standard intramedullary nail-plate constructs have been shown to have lower non-union rates. With decreased non-union rates, re-operation rates will decrease, leading to improved patient outcomes and clinical care. This study will randomize patients to one of the two groups. Then investigators will be collecting data on the standard plate and nail combination and compare outcomes with the Carbofix plate to see differences in union rates. All procedures are currently standard of care and no procedures are research only.

Conditions Studied

Interventions

  • DEVICE Carbo-fix Lateral Plate Device
  • DEVICE Standard Plate-Nail Construct

Study Locations (1)

Missouri

  • University of Missouri-Columbia - Columbia

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-01-29
Est. Completion 2029-12-01
Phase NA

Sponsor

University of Missouri-Columbia

291 total trials

What the Registry Record Tells You About NCT07280169

The ClinicalTrials.gov registry entry for NCT07280169 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 133-participant average among 4 other Distal Femur Fracture trials with a reported enrollment target (25% lower). The listed sponsor is University of Missouri-Columbia, which has 291 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Distal Femur Fracture appearing as the primary indexed condition, and to 2 interventions - of which Carbo-fix Lateral Plate Device is the first listed.

NCT07280169 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT07280169 about?

NCT07280169 is a clinical study titled "Carbo-fix Lateral Plate Devices and Standard Plate-Nail Constructs in Distal Femur Fractures". The purpose of this randomized clinical trial is to decrease non-union rates in distal femur fracture fixation. Carbo-fix lateral femur plate and standard intramedullary nail-plate constructs have been shown to have lower non-union rates. With decreased non-union rates, re-operation rates will decre...

What is the current status of trial NCT07280169?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2026-01-29. Estimated completion is 2029-12-01.

What conditions does trial NCT07280169 study?

This clinical trial studies the following conditions: Distal Femur Fracture.

What interventions are being tested in trial NCT07280169?

The interventions under investigation include: Carbo-fix Lateral Plate Device (DEVICE), Standard Plate-Nail Construct (DEVICE).

Who is sponsoring clinical trial NCT07280169?

This trial is sponsored by University of Missouri-Columbia, which has 291 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07280169 being conducted?

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

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