West Palm Beach, FLNCT06567795Now EnrollingIRB Ready

Diabetes Mellitus Type 2 Clinical Trial in West Palm Beach, FL

Access cutting-edge diabetes mellitus type 2 treatment through this clinical trial at a research site in West Palm Beach. Study-provided care at no cost to qualified participants.

Sponsored by Aventusoft, LLC.

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in West Palm Beach

Access diabetes mellitus type 2 specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related diabetes mellitus type 2 treatment provided free

Apply for This West Palm Beach Location

Check if you qualify for this diabetes mellitus type 2 clinical trial in West Palm Beach, 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 West Palm Beach

    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 West Palm Beach site if eligible
  4. 4Begin participation

About This Diabetes Mellitus Type 2 Study in West Palm Beach

To evaluate the proportion of diabetic mellitus patients with CV events as measured by HEMOTAG.

Sponsor: Aventusoft, LLC.

Who Can Participate

Inclusion Criteria

Adult patients older than 40 years of age.
Diagnosis of Type 2 Diabetes Mellitus (insulin dependent or non-insulin dependent) for at least 5 years.
Diagnosis of Cardiovascular Disease (Coronary Artery Disease, Cerebrovascular Disease, Peripheral Artery Disease, etc…) --OR-- Have one (1) of the following concomitant medical diagnoses:
Diabetic Retinopathy (proliferative or non-proliferative)
Diabetic Nephropathy (eGFR \<60 mL/min/1.73m2 and/or urine albumin/creatinine ratio ≥30 mg/g)
Diabetic Neuropathy
Elevated High-sensitivity C-reactive protein (hs-CRP) --AND-- Have a history of two (2) or more of the following:
Diagnosis of Hypertension for at least 6 months or more (treated or untreated)
Hypercholesterolemia (LDL-C \>100 mg/dL)
Obesity (Body Mass Index (BMI) ≥ 27 for men or ≥ 22 for women)
History of Smoking
Willingness to undergo HEMOTAG evaluation.
Willingness to undergo Standard of Care visits/assessments and NT-pro BNP lab evaluations.
Willingness to conduct at-home HEMOTAG evaluations at least three days per week within a 30-day time period after the completion of the Baseline Visit, after the 6 month visit and following discharge from any hospitalizations due to a cardiac events during the 12 month study period.
Willingness to receive and return shipping of the HEMOTAG KIT at each time point as required by the protocol
Able to give informed consent.

Exclusion Criteria

Terminal condition with life expectancy less than 12 months as determined by investigator.
Physical deformity in the chest area or lesion that may prevent proper HEMOTAG application or adjustment.
Illness/ Condition which may be aggravated or cause significant discomfort to the patient by the application of the HEMOTAG (skin issues, e.g. Intolerance to use of skin electrodes).
Participant enrolled in another interventional study (observational or registries are not excluded).
Prisoners and wards of the state.
Impaired cognitive ability or any other state that may prevent full compliance with the study protocol, according to investigator\'s assessment.
Participants unable to provide informed, voluntary decision to participate in research study as determined by the investigator. (Exclude participants who necessitate the involvement of a legally authorized representative.)
Inability to provide informed consent (Must speak English).
Women who are pregnant or are planning to become pregnant during the study.
Women of childbearing potential who are unwilling or unable to comply with contraception measures.

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 West Palm Beach?

Yes, this clinical trial (NCT06567795) has an active research site in West Palm Beach, 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.

Diabetes Mellitus Type 2 Treatment Options in West Palm Beach, FL

If you're searching for diabetes mellitus type 2 treatment options in West Palm Beach, FL, this clinical trial (NCT06567795) 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 West Palm Beach research site is actively enrolling participants for this clinical trial. You'll receive care from experienced diabetes mellitus type 2 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 diabetes mellitus type 2 clinical trials near you to find additional studies recruiting in your area.

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