Leawood, KSNCT06627673Now EnrollingIRB Ready

Knee Osteoarthritis Clinical Trial in Leawood, KS

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

Sponsored by Maxx Orthopedics Inc

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Expert Care in Leawood

Access knee osteoarthritis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related knee osteoarthritis treatment provided free

Apply for This Leawood Location

Check if you qualify for this knee osteoarthritis clinical trial in Leawood, KS

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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 Leawood

    Convenient for KS 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 Leawood site if eligible
  4. 4Begin participation

About This Knee Osteoarthritis Study in Leawood

The purpose of this investigational device exemption (IDE) study is to monitor the performance (safety and efficacy) of the Maxx Orthopedics, Freedom Total Knee® System, with a femoral component of similar design, manufactured from polyether-ether-ketone (PEEK).

Sponsor: Maxx Orthopedics Inc

Who Can Participate

Inclusion Criteria

Male and female subjects 18 years of age or older.
Subjects with a primary diagnosis of end-stage symptomatic unilateral primary knee osteoarthritis.
Subjects with a pre-operative Knee Society Score (KSS) Knee score of \>25 and \<75.
Subjects who, in the opinion of the Investigator, can understand this clinical investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
Subjects who can give voluntary, written informed consent to participate in this clinical investigation and from whom consent has been obtained.

Exclusion Criteria

Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this clinical investigation.
Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
Subjects who have participated in a clinical study with an investigational product in the last 6 months.
Subjects with other significant disabling problems from the muscular-skeletal system other than in the knees (i.e.: muscular dystrophy, polio, neuropathic joints).
Subjects with known osteoporosis and/or previous history of fracture related to osteoporosis.
Subjects with a current or active history of malignancy, active or suspected infection, Paget's disease, renal osteodystrophy, immunologically suppressed, rheumatoid arthritis, sickle cell anemia, and systemic lupus erythematosus.
Subjects defined by the Investigator as American Society of Anesthesiologists (ASA) Grade III or IV.
Subjects who have a neuromuscular or neurosensory deficit.
Female subjects who are pregnant or lactating.
Subjects with an anatomical limb alignment of above 20 degrees varus or valgus.
Subjects with primary or secondary diagnosis of inflammatory or traumatic arthritis.
Subjects with a fixed flexion deformity of over 20 degrees.
Subjects with recurvatum (definition: hyperextension ≥ 5 degrees).
Subjects who have previously undergone surgery on the indicated knee including total knee arthroplasty, patellofemoral arthroplasty, or unicondylar knee arthroplasty, high tibial osteotomy, ligament reconstruction, fusion, open reduction and internal fixation.
Subjects that have undergone, or scheduled to undergo, contralateral total knee arthroplasty or unicondylar knee arthroplasty within ±1 year from the study surgical procedure.
Evidence of active or suspected (systemic or local) infection at time of surgery.

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 Leawood?

Yes, this clinical trial (NCT06627673) has an active research site in Leawood, KS 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 Osteoarthritis Treatment Options in Leawood, KS

If you're searching for knee osteoarthritis treatment options in Leawood, KS, this clinical trial (NCT06627673) 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 Leawood research site is actively enrolling participants for this clinical trial. You'll receive care from experienced knee osteoarthritis 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.

Looking for more options? Browse all knee osteoarthritis clinical trials near you to find additional studies recruiting in your area.

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