Golden, CONCT04984291Now EnrollingIRB Ready

Shoulder Fractures Clinical Trial in Golden, CO

Access cutting-edge shoulder fractures treatment through this clinical trial at a research site in Golden. Study-provided care at no cost to qualified participants.

Sponsored by Zimmer Biomet

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Expert Care in Golden

Access shoulder fractures specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related shoulder fractures treatment provided free

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Check if you qualify for this shoulder fractures clinical trial in Golden, CO

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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 Golden

    Convenient for CO 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 Golden site if eligible
  4. 4Begin participation

About This Shoulder Fractures Study in Golden

The objectives of this study are to confirm the safety, performance, and clinical benefits of Zimmer Biomet Shoulder Arthroplasty Systems and its instrumentation in primary or revision shoulder arthroplasty. These objectives will be assessed using standard scoring systems, radiographic evidence, and adverse event records. Safety of the system will be assessed by monitoring the frequency an incidence of adverse events.

Sponsor: Zimmer Biomet

Who Can Participate

Inclusion Criteria

Patient must be 20 years of age or older.
Patient must be anatomically and structurally suited to receive shoulder arthroplasty implants.
Patient is a candidate for shoulder arthroplasty due to one or more of the following:
Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis.
Rheumatoid arthritis.
Correction of functional deformity.
Fractures of the proximal humerus, where other methods of treatment are deemed inadequate.
Difficult clinical management problems, where other methods of treatment may not be suitable or may be inadequate.
Patient must be able and willing to complete the protocol required follow-up.
Patient must be able and willing to sign the IRB/EC approved informed consent.
Patient has grossly deficient rotator, (for reverse application)
With severe arthropathy and/or
Previously failed shoulder joint replacement
Patient must have functional deltoid muscle (for reverse application)

Exclusion Criteria

Patient is unwilling or unable to give consent or to comply with the follow-up program.
Patient has any condition which would in the judgement of the Investigator, place the patient at undue risk or interfere with the study.
Patient is known to be pregnant or breastfeeding.
Patient is a vulnerable subject (prisoner, mentally incompetent or unable to understand what participation to the study entails, a known alcohol or drug abuser, and/or anticipated to be non-compliant).
Patient is uncooperative or patient with neurologic disorders who is incapable or unwilling to follow directions.
Patient has any sign of infection affecting the shoulder joint or in its proximity which may spread to the implant site.
Patient has rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram.
Patient has any neuromuscular disease compromising the affected limb that would render the procedure unjustifiable.
Patient presents with osteoporosis, which in the opinion of the Investigator, may limit the subject's ability to support total shoulder arthroplasty using the study device.
Patient has osteomalacia.
Patient has a metabolic disorder that may impair bone formation.
Patient has deficient rotator cuff.
Patient presents with significant injury to the upper brachial plexus.
Patient has paralysis of the axillary nerve.
Patient has non-functional deltoid or external rotator muscles.

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 Golden?

Yes, this clinical trial (NCT04984291) has an active research site in Golden, CO 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.

Shoulder Fractures Treatment Options in Golden, CO

If you're searching for shoulder fractures treatment options in Golden, CO, this clinical trial (NCT04984291) 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 Golden research site is actively enrolling participants for this clinical trial. You'll receive care from experienced shoulder fractures 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 shoulder fractures clinical trials near you to find additional studies recruiting in your area.

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