Chicago, ILNCT06918041Now EnrollingIRB Ready

Rotator Cuff Tear Clinical Trial in Chicago, IL

Access cutting-edge rotator cuff tear treatment through this clinical trial at a research site in Chicago. Study-provided care at no cost to qualified participants.

Sponsored by ZuriMED Technologies Inc.

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Expert Care in Chicago

Access rotator cuff tear specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related rotator cuff tear treatment provided free

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Check if you qualify for this rotator cuff tear clinical trial in Chicago, IL

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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 Chicago

    Convenient for IL 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 Chicago site if eligible
  4. 4Begin participation

About This Rotator Cuff Tear Study in Chicago

The purpose of this study is to prospectively evaluate healing, functional clinical outcomes, and safety of arthroscopic rotator cuff repairs augmented with the FiberLocker® System (encompassing the SpeedPatch® PET and the FiberLocker® Instrument). The primary outcome measure is healing evaluation based on Magnetic Resonance Imaging (MRI) at a minimum of 6 months post-operatively. The secondary outcome measures are the Sugaya classification, Goutallier Stage and tendon quality based on MRI as well as objective scores and patient-reported outcome measures (PROMs) from validated outcome scoring systems.

Sponsor: ZuriMED Technologies Inc.

Who Can Participate

Inclusion Criteria

The Subject is between the ages of 30 and 70 years.
Subject is planning to undergo arthroscopic surgery for full-thickness rotator cuff tear (RCT)
Tear size ≥ 2 cm
Primary rotator cuff repair
Subject preoperative MRI obtained within 1 year prior to surgery

Exclusion Criteria

The Subject is unable or unwilling to sign the Patient Informed Consent, approved by the Institutional Review Board.
The Subject objects to the use of the FiberLocker® System
History or known allergy or intolerance to polyester
Complete full-thickness subscapularis tears of \> than the superior 1/3 of the tendon (Lafosse grade 3 and above)
Hamada grade III and above
Less than 2 mm joint space of the glenohumeral joint on either an anteroposterior or axillary radiograph
Recurrent shoulder instability
Corticosteroid injection in the operative shoulder within three months before surgery
Subjects with inflammatory or auto-immune based joint diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus)
Subjects with current acute infection in the area surrounding the surgical site
Revision rotator cuff repair
Pregnant or planning to become pregnant during the study period
Subject is breastfeeding during the study period
Subject has conditions or circumstances that would interfere with study requirements
The subject's condition represents a worker's compensation case Intraoperative Exclusion Criteria:
Partial rotator cuff repairs
Lafosse grade 3 or higher subscapularis tears
Limited space for implant delivery
FiberLocker® System cannot be used as indicated

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 Chicago?

Yes, this clinical trial (NCT06918041) has an active research site in Chicago, IL 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.

Rotator Cuff Tear Treatment Options in Chicago, IL

If you're searching for rotator cuff tear treatment options in Chicago, IL, this clinical trial (NCT06918041) 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 Chicago research site is actively enrolling participants for this clinical trial. You'll receive care from experienced rotator cuff tear 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 rotator cuff tear clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Chicago, IL