Jacksonville, FLNCT06752577Now EnrollingIRB Ready

Chronic Kidney Diseases Clinical Trial in Jacksonville, FL

Access cutting-edge chronic kidney diseases treatment through this clinical trial at a research site in Jacksonville. Study-provided care at no cost to qualified participants.

Sponsored by Mayo Clinic

Quick Self-Assessment

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Expert Care in Jacksonville

Access chronic kidney diseases specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic kidney diseases treatment provided free

Apply for This Jacksonville Location

Check if you qualify for this chronic kidney diseases clinical trial in Jacksonville, FL

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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 Jacksonville

    Convenient for FL 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 Jacksonville site if eligible
  4. 4Begin participation

About This Chronic Kidney Diseases Study in Jacksonville

The purpose of this protocol is to treat an intermediate-sized population with chronic kidney disease (CKD) including kidney transplant recipients. The protocol uses allogeneic bone marrow-derived mesenchymal stem cells (MSCs). MSC infusion may be delivered 1) intravenous or 2) intravenous plus intra-arterial to both kidneys. Individuals will have subsequent follow up for safety evaluations. Repeat dosing is allowed.

Sponsor: Mayo Clinic

Who Can Participate

Inclusion Criteria

Age \>18 years
Estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73m2
Hemoglobin A1c ≤9%, if diabetes mellitus present
If kidney transplant recipient, must have eGFR\<60 mL/min/1.73m2 and evidence of progressive kidney function loss over ≥6 months
Ability to give informed consent

Exclusion Criteria

Anemia (hemoglobin \<8.5 g/dL)
Body weight \>150 kg or BMI \>50
Uncontrolled hypertension: sustained systolic blood pressure (SBP) \>160 mmHg or diastolic blood pressure (DBP) ≥100 mmHg despite maximal doses of at least 2 different classes of anti-hypertensive medications
Chronic hypotension history: sustained SBP \<85 mmHg
Kidney failure requiring ongoing kidney replacement therapy including hemodialysis or peritoneal dialysis
Active, high-dose immunosuppression therapy (e.g. chronic prednisone ≥20 mg daily)
Solid organ transplantation history; excluding kidney transplant
Active treatment for acute cellular rejection, in kidney transplant recipients
Recent cardiovascular event (hospitalization for myocardial infarction, stroke, congestive heart failure (NYHA class ≥III or ejection fraction ≤30%) within 3 months or uncontrolled cardiac arrhythmias (e.g. ventricular arrhythmia, supraventricular tachycardia and bradyarrhythmia)
History of liver cirrhosis
Chronic obstructive pulmonary disease or asthma requiring daily medication
History of recurring blood clotting disorder (thromboembolism: pulmonary embolism, deep venous thrombosis) requiring chronic anticoagulation therapy
Unwilling to use contraception for at least 2 months after MSC infusion if sexually active and able to become pregnant or father a child.
Active malignancy
Active infection (e.g. systemic or specific organ involvement such as pneumonia or osteomyelitis; in kidney transplant recipients, active BK nephropathy)
Recent COVID-19 infection, within the last 1 month
History of hepatitis B or C (without cure), or HIV infection
History of allergic reaction to cellular products (i.e. blood transfusions, platelets)
Active tobacco use
Illicit drug use and excessive alcohol use
Presence of psychosocial issues (e.g., uncontrolled mental illness, unpredictable childcare or eldercare responsibilities, irregular/ inflexible work schedule) that may interfere with the ability to complete all study procedures
Anticipating prolonged travel or other physical restrictions that would prohibit return for scheduled study visits.
Inability to give informed consent

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 Jacksonville?

Yes, this clinical trial (NCT06752577) has an active research site in Jacksonville, FL 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.

Chronic Kidney Diseases Treatment Options in Jacksonville, FL

If you're searching for chronic kidney diseases treatment options in Jacksonville, FL, this clinical trial (NCT06752577) 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 Jacksonville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic kidney diseases 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 chronic kidney diseases clinical trials near you to find additional studies recruiting in your area.

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