San Antonio, TXNCT06446531Now EnrollingIRB Ready

Pre-Diabetes Clinical Trial in San Antonio, TX

Access cutting-edge pre-diabetes treatment through this clinical trial at a research site in San Antonio. Study-provided care at no cost to qualified participants.

Sponsored by The University of Texas Health Science Center at San Antonio

Quick Self-Assessment

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Expert Care in San Antonio

Access pre-diabetes specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related pre-diabetes treatment provided free

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Check if you qualify for this pre-diabetes clinical trial in San Antonio, TX

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to San Antonio

    Convenient for TX 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 San Antonio site if eligible
  4. 4Begin participation

About This Pre-Diabetes Study in San Antonio

The investigators are studying how to help people with prediabetes (Pre-DM) and obesity. The goal is to use new and affordable treatments to bring blood sugar levels back to normal and help participants to lose weight. The investigators also want to reduce participants risk of heart problems. The study team will look at how these treatments affect metabolism and other body functions to help find new ways to treat diabetes and obesity in the future.

Sponsor: The University of Texas Health Science Center at San Antonio

Who Can Participate

Inclusion Criteria

Patients will have an established diagnosis of pre-Diabetes Mellitus (DM) before the screening visit, documented by an acceptable modality in the last 6 months.
Age ≥ 18 years old
Body Mass Index (BMI)=25-40 kg/m2
Glycated Hemoglobin (HbA1c) = 5.7-6.4%
Blood Pressure (BP) \<160/100
Estimated Glomerular Filtration Rate (eGFR) ≥30 ml/min•1.73m2
Body weight must be stable (±5 pounds) over the last 3 months.
Oral diuretics, if prescribed to the patient according to local guidelines and discretion of the investigator, should be stable for at least 1 week prior to randomization.
Hispanic ethic group
Willing to adhere to medication regimen for up to 6 months.
Male or female, if female, met these criteria:
Not pregnant or breast-feeding
Negative pregnancy test result at visit 1 (screening)
During the entire study, women of childbearing potential (WOCBP) including peri-menopausal women who have a menstrual period within 1 year must practice appropriate, and effective birth control, either implants or pills, or a vasectomized partner prior to receiving the first dose of study medication
Does not suffer from severe claustrophobia
No contraindication for Magnetic Resonance Imaging (MRI) (metal plates, screws, shrapnel, pins, or cardiac pacemaker)

Exclusion Criteria

Patients currently on one of the selected therapies
Extended diagnoses with Type 2 Diabetes
Pregnancy, lactation, women of childbearing age (WOCBA) unwilling to use contraception
Known allergy/sensitivity to study drugs or their ingredients
Major oncologic diagnosis in the last 5 years
Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
Inability or unwillingness of individual or legal guardian/representative to give written informed consent
Major organ or metabolic diseases, or physical limitations that will not allow the subject to complete the study
Myocardial infraction, coronary artery bypass graft surgery, or other major cardiovascular event in the past 60 days
Heart transplant recipient or listed for a heart transplant
Currently implanted left ventricular assist device
Cardiomyopathy based on infiltrative or cumulative hypertrophic obstructive cardiomyopathy or known pericardial constriction
Any severe (obstructive or regurgitant) valvular heart disease, expected to lead to surgery during the trial period
Acute decompensated heart failure requiring intravenous diuretics, vasodilators, inotropic agents, or mechanical support within 1 week of screening and during the screening period prior to randomization
Implanted cardioverter defibrillator within 3 months prior to screening
Cardiac resynchronization therapy

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 San Antonio?

Yes, this clinical trial (NCT06446531) has an active research site in San Antonio, TX 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.

Pre-Diabetes Treatment Options in San Antonio, TX

If you're searching for pre-diabetes treatment options in San Antonio, TX, this clinical trial (NCT06446531) 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 San Antonio research site is actively enrolling participants for this clinical trial. You'll receive care from experienced pre-diabetes 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 pre-diabetes clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · San Antonio, TX