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RECRUITING NA

Femoral BMD Change Following Cemented or Cementless Total Knee Arthroplasty

NCT06733597 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to examine femur bone mineral density (BMD) change before and after surgery in patients receiving cemented or cementless total knee arthroplasty (TKA). performed with manual or robotic methods. 100 participants will be enrolled and can expect to be on study for up to 26 months.

Conditions Studied

Interventions

  • PROCEDURE Cement
  • OTHER Cementless
  • PROCEDURE Manual Surgery
  • PROCEDURE Robotic Surgery

Study Locations (1)

Wisconsin

  • UW School of Medicine and Public Health — Madison

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-03-06
Est. Completion 2028-06
Phase NA

Sponsor

University of Wisconsin, Madison

943 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06733597

The ClinicalTrials.gov registry entry for NCT06733597 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 943 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 Knee Arthropathy appearing as the primary indexed condition, and to 4 interventions — of which Cement 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: NCT06733597 reports 1 study location spanning 1 distinct geographic area — top geographies include Wisconsin. 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 NCT06733597 about?

NCT06733597 is a clinical study titled "Femoral BMD Change Following Cemented or Cementless Total Knee Arthroplasty". The purpose of this study is to examine femur bone mineral density (BMD) change before and after surgery in patients receiving cemented or cementless total knee arthroplasty (TKA). performed with manual or robotic methods. 100 participants will be enrolled and can expect to be on study for up to 26 ...

What is the current status of trial NCT06733597?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-03-06. Estimated completion is 2028-06.

What conditions does trial NCT06733597 study?

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

What interventions are being tested in trial NCT06733597?

The interventions under investigation include: Cement (PROCEDURE), Cementless (OTHER), Manual Surgery (PROCEDURE), Robotic Surgery (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06733597?

This trial is sponsored by University of Wisconsin, Madison, which has 943 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06733597 being conducted?

This trial has 1 study location across Wisconsin. 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