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ACTIVE NOT RECRUITING

A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis

NCT05197036 · View on ClinicalTrials.gov ↗

Study Summary

A clinical trial investigating the safety and effectiveness of Smith and Nephew's FDA-approved Porous Total Knee System, which is used to replace worn away and diseased knee joints. The aim of this study is to show that most patients who receive the Porous Total Knee System have reduced pain, greater mobility and a long-lasting implant post-surgery.

Interventions

  • PROCEDURE Total Knee Arthroplasty

Study Locations (18)

New York

  • Syracuse Orthopedic Specialists — East Syracuse
  • NYU Langone Health Orthopedic Hospital — New York
  • Columbia University — New York

Georgia

  • Emory Orthopaedics and Spine Hospital — Atlanta

Massachusetts

  • Massachusetts General Hospital — Boston

Michigan

  • The Core Institute — Novi

North Carolina

  • Duke Health — Morrisville

Oregon

  • Oregon Health & Science University — Portland

South Carolina

  • Medical University of South Carolina — Charleston

Tennessee

  • Erlanger Health — Chattanooga

Trial Details

FieldValue
Enrollment Target 299 participants
Start Date 2021-12-21
Est. Completion 2033-12-25

Sponsor

Smith & Nephew

52 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05197036

The ClinicalTrials.gov registry entry for NCT05197036 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 299 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Smith & Nephew, which has 52 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Rheumatoid Arthritis appearing as the primary indexed condition, and to 1 intervention — of which Total Knee Arthroplasty 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: NCT05197036 reports 18 study locations spanning 16 distinct geographic areas — top geographies include New York, Georgia, Massachusetts. 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 NCT05197036 about?

NCT05197036 is a clinical study titled "A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis". A clinical trial investigating the safety and effectiveness of Smith and Nephew's FDA-approved Porous Total Knee System, which is used to replace worn away and diseased knee joints. The aim of this study is to show that most patients who receive the Porous Total Knee System have reduced pain, greate...

What is the current status of trial NCT05197036?

This trial is currently active not recruiting. The enrollment target is 299 participants. The study started on 2021-12-21. Estimated completion is 2033-12-25.

What conditions does trial NCT05197036 study?

This clinical trial studies the following conditions: Rheumatoid Arthritis, Osteoarthritis, Post-traumatic Arthritis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05197036?

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

Who is sponsoring clinical trial NCT05197036?

This trial is sponsored by Smith & Nephew, which has 52 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05197036 being conducted?

This trial has 18 study locations across Georgia, Massachusetts, Michigan, New York, North Carolina. 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