ACL Reconstruction, Anterior Cruciate Ligament Rupture, Meniscus Tears
Conditions
Keywords
ACL, Meniscus tear, ACL tear, Compression sleeve, Semiconductor fabric, ACL reconstruction
Brief summary
The goal of this clinical trial is to determine the effect of semiconductor sleeves on the treatment of Anterior Cruciate Ligament (ACL) or Anterior Cruciate Ligament and Meniscus (ACL+Meniscus) arthroscopic surgery. The effect of the sleeves will be analyzed through patient reported and clinically measured outcomes. The main questions it aims to answer are: * Do the semiconductor sleeves improve the functional outcomes compared to the placebo? * Will patients experience improved functional outcomes in a shorter period of time compared to the placebo? Researchers will compare semiconductor fabric sleeves to a placebo (a look-alike sleeve that contains no semiconductor material) to see if the semiconductor fabric better treats ACL and ACL+meniscus surgical patients. Participants will: * Wear semiconductor or placebo leg sleeve for 4 weeks and knee sleeve for the following 12 weeks * Complete patient reported outcome surveys
Interventions
DEVICESemiconducting fabric sleeves
This intervention includes semiconductor embedded sleeves that patients will wear for 4 months post-operatively.
DEVICENon-semiconducting fabric sleeves
This intervention includes sleeves absent of semiconductors that will be worn for 4 months post-operatively.
Sponsors
INCREDIWEAR HOLDINGS, INC.
Illinois Center for Orthopaedic Research and Education
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Patients undergoing ACL or ACL+Meniscus surgery * Age 16 - 65 * Patients with Body Mass Index (BMI) \<40 * Patients who are willing and able to adhere to follow-up schedule and protocol guidelines. * Patients who are willing and able to sign corresponding research subject consent/assent form.
Exclusion criteria
* Patient has a history of neurological conditions, including multiple sclerosis or Parkinson's disease * Patient has severe medical condition, including recent myocardial infarction, unstable angina, heart failure, severe anemia * Patient has had prior surgical treatment of the knee in the last 5 years or injection treatment(s) in the last 6 months * Patient has chronic pain conditions unrelated to knee condition * Patient has auto-immune or auto-inflammatory diseases * Patient has poorly controlled diabetes (HgA1c \> 7.5) * Patient has BMI \> 39.9 * Patient has varicosities on the operative leg * Patient has severe peripheral artery disease (ABI \< 0.6) * Patient is considered a pain management patient * Patient has had previous blood clots or stroke * Patient has used tobacco within the last 90 days * Patient is not within the ages of 16-65 * Patient has an active infection (local or systemic), or an open (non-surgical) wound in the areas of product application * Patient is unwilling or unable to sign the corresponding research subject consent/assent form * Patient meets any other criteria or has any other condition that, in the opinion of the investigator, would prevent them from completing the study or that, in the opinion of the investigator, would confound study results.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Range of motion | 1 year | Measured extension and flexion values using a goniometer at baseline, 2 weeks, 6 weeks, 3 months, 6 months, and 1 year time points |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Effusion Measurements | 1 year | Effusion is measured by taking the circumference using a soft measuring tape at the following points: 1. Mid thigh: distance from palpation of Anterior Superior Iliac Spine (ASIS) to superior pole of patella, divided in half. (cm) 2. Knee: midpoint of the patella. (cm) 3. Mid calf: distance from top of fibular head to bottom of lateral malleolus, divided in half. (cm) |
| Secondary Outcome Measures using Validated patient-reported outcome tools questionnaires | 1 year | Visual Analog Scale (VAS) - assess pain, It is a 0-100 scale. A higher score indicates greater pain intensity. |
Countries
United States
Contacts
Primary ContactRonak M Patel, MD
Outcome results
None listed