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Knee Flexionater to Avoid Motion Restoring Surgery

Ermi LLC · NCT07454356

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 40+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
150
US sites recruiting
1
Study start
December 9, 2025
Record last updated
March 6, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Hydraulic high Intensity Stretch Device; Standard Physical Therapy

Conditions: Joint Contractures; Total Knee Anthroplasty; Knee Arthrofibrosis

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Age 40 years or older
  • Undergoing primary total knee replacement surgery
  • Knee flexion less than 105 degrees at approximately 4 weeks after surgery
  • Considered a candidate for motion-restoring surgery, with any surgery delayed until after 2 months of nonoperative treatment

Exclusion Criteria

  • Not willing to participate
  • Diagnosis of advanced rheumatoid arthritis
  • Neurological deficit affecting the operative leg
  • Revision total knee replacement or previous major surgery on the same knee
  • Cognitive impairment
  • Prior total hip replacement on the same side (ipsilateral total hip arthroplasty)
  • Living more than 2 hours from the study site or unwilling to attend required local physical therapy visits

Recruiting US locations

  • INOV8 Orthopedics

    Houston, TX 77043

    Site contact: Director of Research · 832-240-5974 · bpeace@inov8hc.com

Knee Flexionater to Avoid Motion Restoring Surgery (NCT07454356) | Bored Studies