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NCT07454356 · ClinicalTrials.gov registry record · NA
Knee Flexionater to Avoid Motion Restoring Surgery
A NA study of Joint Contractures and Total Knee Anthroplasty, sponsored by Ermi.
- Recruiting
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT07454356 is a NA study of Joint Contractures and Total Knee Anthroplasty that is actively recruiting participants, run by Ermi. The registered enrollment target is 150 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07454356, a NA study of Joint Contractures and Total Knee Anthroplasty, is actively recruiting participants, sponsored by Ermi.
- RECRUITING
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn whether adding a stretching device to standard physical therapy can help people regain knee bending after total knee replacement surgery. Some people have difficulty bending their knee during recovery. When this happens, doctors may recommend another procedure called motion-restoring surgery to improve knee movement. This study aims to answer two main questions. First, does adding a hydraulic high-intensity stretching device to physical therapy help people regain knee bending after surgery? Second, does using the device affect recovery, daily activities, or the chance of needing another procedure? Researchers will compare two treatment approaches. One group will receive standard physical therapy alone. The other group will receive standard physical therapy and will also use a hydraulic high-intensity stretching device called the Ermi Knee Flexionater at home. Participants who receive the device will use it at home each day in addition to attending their physical therapy sessions. Researchers will measure how well participants can bend their knee and will ask questions about pain, daily function, and activity level. Participants will also complete simple walking and mobility tests. Study visits will occur about four weeks after surgery when participants enroll, and again at about eight weeks, twelve weeks, six months, one year, and two years after surgery. Researchers will compare results between the two groups to see whether the stretching device improves recovery after knee replacement.
Conditions Studied
Interventions
- OTHER Standard Physical Therapy
- DEVICE Hydraulic high Intensity Stretch Device
Study Locations (1)
Texas
- INOV8 Orthopedics - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2025-12-09 |
| Est. Completion | 2029-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07454356
The ClinicalTrials.gov registry entry for NCT07454356 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ermi, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Joint Contractures appearing as the primary indexed condition, and to 2 interventions - of which Standard Physical Therapy is the first listed.
NCT07454356 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT07454356 about?
NCT07454356 is a clinical study titled "Knee Flexionater to Avoid Motion Restoring Surgery". The goal of this clinical trial is to learn whether adding a stretching device to standard physical therapy can help people regain knee bending after total knee replacement surgery. Some people have difficulty bending their knee during recovery. When this happens, doctors may recommend another proc...
What is the current status of trial NCT07454356?
This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2025-12-09. Estimated completion is 2029-12.
What conditions does trial NCT07454356 study?
This clinical trial studies the following conditions: Joint Contractures, Total Knee Anthroplasty, Knee Arthrofibrosis.
What interventions are being tested in trial NCT07454356?
The interventions under investigation include: Standard Physical Therapy (OTHER), Hydraulic high Intensity Stretch Device (DEVICE).
Who is sponsoring clinical trial NCT07454356?
This trial is sponsored by Ermi, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07454356 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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