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ACTIVE NOT RECRUITING

Prospective Evaluation of ProChondrix CR for Repair of Articular Cartilage Defects on Femoral Condyle and Patella

NCT03873545 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this clinical study is to evaluate the use of ProChondrix Cryopreserved Osteochondral Allograft to obtain evidence of effectiveness, defined as an improvement in physical function and pain, when used on a symptomatic cartilage defect on the femoral condyle or patella in a mechanically stable knee.

Interventions

  • PROCEDURE Cryopreserved Osteochondral Allograft

Study Locations (3)

Illinois

  • Midwest Orthopaedics at Rush — Chicago

Kentucky

  • University of Kentucky Research Foundation — Lexington

Ohio

  • Beacon Orthopaedics & Sports Medicine — Cincinnati

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2019-03-18
Est. Completion 2028-12-30

Sponsor

AlloSource

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03873545

The ClinicalTrials.gov registry entry for NCT03873545 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AlloSource, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Cartilage Injury appearing as the primary indexed condition, and to 1 intervention — of which Cryopreserved Osteochondral Allograft 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: NCT03873545 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Illinois, Kentucky, 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 NCT03873545 about?

NCT03873545 is a clinical study titled "Prospective Evaluation of ProChondrix CR for Repair of Articular Cartilage Defects on Femoral Condyle and Patella". The purpose of this clinical study is to evaluate the use of ProChondrix Cryopreserved Osteochondral Allograft to obtain evidence of effectiveness, defined as an improvement in physical function and pain, when used on a symptomatic cartilage defect on the femoral condyle or patella in a mechanically...

What is the current status of trial NCT03873545?

This trial is currently active not recruiting. The enrollment target is 34 participants. The study started on 2019-03-18. Estimated completion is 2028-12-30.

What conditions does trial NCT03873545 study?

This clinical trial studies the following conditions: Cartilage Injury, Cartilage Damage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03873545?

The interventions under investigation include: Cryopreserved Osteochondral Allograft (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03873545?

This trial is sponsored by AlloSource, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03873545 being conducted?

This trial has 3 study locations across Illinois, Kentucky, 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