A Study to Evaluate the Incrediwear Products Immediately After ACL Repair

Enrolling by invitation · Not applicable · Has a placebo group

Conditions studied: Anterior Cruciate Ligament Tear, Medial Collateral Ligament

In brief

To assess the benefits of using the Incrediwear knee products after ACL or ACL+MCL arthroscopic surgery, on the postoperative pain, range of motion and effusion. The study team will compare patients with Incrediwear products, or placebo Incrediwear products, or no products during the first 6-month postoperative period. The group that does not wear the Incrediwear or placebo products is considered the standard of care control group and will proceed with the normal standard of care compression hose.

Key facts

Study ID

NCT06668376

Run by

Texas Bone and Joint

People needed

90

Starts

2024-10-29

Expected to finish

2026-11-01

Last updated by the study team

2024-11-01

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Consented to protocol
• Compliant protocol
• BMI less than 35
• Undergoing ACL or ACL+MCL within 30 days

You may not qualify if…

• Pregnancy
• 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

Where it is running

• Medical City Denton — Denton, Texas, United States

Full record on ClinicalTrials.gov

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