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NCT06733597 · ClinicalTrials.gov registry record · NA

Femoral BMD Change Following Cemented or Cementless Total Knee Arthroplasty

A NA study of Knee Arthropathy, sponsored by University of Wisconsin, Madison.

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

NCT06733597 is a NA study of Knee Arthropathy that is actively recruiting participants, run by University of Wisconsin, Madison. The registered enrollment target is 100 participants, below the 156-participant average among 4 other Knee Arthropathy trials with a reported enrollment target (36% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06733597, a NA study of Knee Arthropathy, is actively recruiting participants, sponsored by University of Wisconsin, Madison.

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

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

1,039 total trials

What the Registry Record Tells You About NCT06733597

The ClinicalTrials.gov registry entry for NCT06733597 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 156-participant average among 4 other Knee Arthropathy trials with a reported enrollment target (36% lower). The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.

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.

NCT06733597 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.

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.

What interventions are being tested in trial NCT06733597?

The interventions under investigation include: Cement (PROCEDURE), Cementless (OTHER), Manual Surgery (PROCEDURE), Robotic Surgery (PROCEDURE).

Who is sponsoring clinical trial NCT06733597?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.

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.

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

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