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RECRUITING NA

Rim Plate to Buttress Plate for Posterior Wall Acetabular Fractures With and Without Inter-fragmentary Screws

NCT06409559 · View on ClinicalTrials.gov ↗

Study Summary

The hypothesis of this study is that the Rim Plate method utilizing interfragmentary screws placed through the plate will result in superior fixation, a lower rate of loss of reduction of the fracture fragment, better anatomic healing of the articular (joint) surface, a decreased rate of early post-traumatic arthritic changes of the joint (cartilage) surface, and improved functional outcomes.

Conditions Studied

Interventions

  • DEVICE Pelvic reconstruction plate without interfragmentary screws
  • DEVICE Pelvic reconstruction plate with interfragmentary screws

Study Locations (1)

Ohio

  • University of Cincinnati College of Medicine — Cincinnati

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2023-08-01
Est. Completion 2028-03
Phase NA

Sponsor

University of Cincinnati

179 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06409559

The ClinicalTrials.gov registry entry for NCT06409559 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Cincinnati, which has 179 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acetabular Fracture appearing as the primary indexed condition, and to 2 interventions — of which Pelvic reconstruction plate without interfragmentary screws is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06409559 reports 1 study location spanning 1 distinct geographic area — top geographies include Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06409559 about?

NCT06409559 is a clinical study titled "Rim Plate to Buttress Plate for Posterior Wall Acetabular Fractures With and Without Inter-fragmentary Screws". The hypothesis of this study is that the Rim Plate method utilizing interfragmentary screws placed through the plate will result in superior fixation, a lower rate of loss of reduction of the fracture fragment, better anatomic healing of the articular (joint) surface, a decreased rate of early post-...

What is the current status of trial NCT06409559?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2023-08-01. Estimated completion is 2028-03.

What conditions does trial NCT06409559 study?

This clinical trial studies the following conditions: Acetabular Fracture. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06409559?

The interventions under investigation include: Pelvic reconstruction plate without interfragmentary screws (DEVICE), Pelvic reconstruction plate with interfragmentary screws (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06409559?

This trial is sponsored by University of Cincinnati, which has 179 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06409559 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial