Incrediwear ACL MCL Arthroscopic Surgery Recovery Study
Enrolling by invitation · Not applicable · Has a placebo group
Conditions studied: Arthroscopic Surgical Procedures, Anterior Cruciate Ligament Reconstruction
In brief
The goal of this clinical trial is to assess the benefits of using the Incrediwear knee products after anterior cruciate ligament arthroscopic surgery or anterior cruciate ligament and medial collateral ligament (ACL+MCL) arthroscopic surgery, on the postoperative pain, range of motion and effusion. Participant population includes female or male patients in relative good health, 18 to 65 years old. The investigators will compare participants with Incrediwear and placebo Incrediwear products during the first 6-month postoperative period. The main question it aims to answer are: * Will the Incrediwear products help participants to decrease postoperative pain and swelling? * Will the Incrediwear products help the participants by increasing the range of motion in a shorter amount of time than the placebo group? Participants will be asked to maintain a journal documenting surgical site pain, pain medication type and quantity taken. Researcher will compare 90 participants enrolled in one of six groups, double blinded and randomly assigned, to see if the Incrediwear products assist in controlling postoperative swelling, and increase range of motion in a shorter amount of time. * ACL participants randomly assigned the Incrediwear product, placebo product, or none * ACL+MCL participants randomly assigned the Incrediwear product, placebo product, or none
Key facts
- Study ID
- NCT06240780
- Run by
- Oklahoma Joint Reconstruction Institute
- People needed
- 90
- Starts
- 2024-08-30
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2025-09-30
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Consented to protocol
- Compliant to protocol
- BMI less than 35
- Undergoing ACL or ACL+MCL within 30 days
You may not qualify if…
- Rheumatoid Arthritis
- Poorly controlled diabetes (HgA1c > 7.5)
- Previous blood clots
- BMI greater than 35
- Varicosities on operative leg
- Pain management patient
- Prior knee surgery to the operative / study knee
- Worker's Comp patients
- Pregnancy
Where it is running
- Oklahoma Joint Reconstruction Institute — Oklahoma City, Oklahoma, United States
Full record on ClinicalTrials.gov
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