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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: Recruiting NA study of Knee Arthropathy, sponsored by University of Wisconsin, Madison.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Primary endpoint is to estimate percent BMD change 12 and 24 months after TKA at the distal femur, 25 percent region of interest, reported for all participants together.
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
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-03-06 |
| Est. Completion | 2028-06 |
| Phase | NA |
What NCT06733597 shows while recruiting
NCT06733597 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 156-participant average among 4 other Knee Arthropathy trials with a reported enrollment target (36% lower).
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 a single indexed study location in 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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