Akron, OHNCT03588975Now EnrollingIRB Ready

Knee Cartilage Damage Clinical Trial in Akron, OH

Access cutting-edge knee cartilage damage treatment through this clinical trial at a research site in Akron. Study-provided care at no cost to qualified participants.

Sponsored by Vericel Corporation

Quick Self-Assessment

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Expert Care in Akron

Access knee cartilage damage specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related knee cartilage damage treatment provided free

Apply for This Akron Location

Check if you qualify for this knee cartilage damage clinical trial in Akron, OH

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Akron

    Convenient for OH residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Akron site if eligible
  4. 4Begin participation

About This Knee Cartilage Damage Study in Akron

The objective of this study is to compare the efficacy and safety of MACI® vs arthroscopic microfracture in the treatment of patients aged 10 to 17 years with symptomatic articular chondral or osteochondral defects of the knee.

Sponsor: Vericel Corporation

Who Can Participate

Inclusion Criteria

Symptomatic cartilage or osteochondral defects
One or more International Cartilage Repair Society (ICRS) Grade III or IV chondral or unsalvageable osteochondral defects located on the femoral condyles and/or trochlea amenable to treatment with the surgical procedure determined at randomization (MACI or microfracture).
At least 1 defect size ≥1.5 cm2 on the femoral condyles and/or the trochlea; defects include OCD lesions with a bone lesion depth of ≤6 mm and does not require a bone graft.
Stable target knee (i.e., anterior and posterior cruciate ligaments should be free of laxity as well as stable and intact). Ligament repair or reconstruction procedures are allowed prior to screening arthroscopy.
Intact meniscus or partial meniscus (at least 50% of functional meniscus remaining) in the target knee.

Exclusion Criteria

Any surgery on the target knee joint within 6 months prior to Screening (not including diagnostic arthroscopy)
ICRS Grade III or IV

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Akron?

Yes, this clinical trial (NCT03588975) has an active research site in Akron, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Knee Cartilage Damage Treatment Options in Akron, OH

If you're searching for knee cartilage damage treatment options in Akron, OH, this clinical trial (NCT03588975) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Akron research site is actively enrolling participants for this clinical trial. You'll receive care from experienced knee cartilage damage specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

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Take the first step toward participating in this groundbreaking clinical trial

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