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NCT06355310 · Justin Ryder

Mechanisms of SGLT2 Inhibition in Pediatric Steatotic Liver Disease

(SHIELD)

What this study is about

This study is a randomly assigned, where neither patients nor doctors know which treatment is given, compared against an inactive treatment trial specifically designed to evaluate the preliminary feasibility, initial effectiveness and safety of SGLT2 inhibitors for treating NAFLD in adolescents with obesity.

View original scientific description

This study is a randomized, double-blind, placebo-controlled trial specifically designed to evaluate the preliminary feasibility, initial efficacy and safety of SGLT2 inhibitors for treating NAFLD in adolescents with obesity.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • For clinical referral to screening visit:
  • BMI \>30 kg/m2 or \>95th BMI-Percentile
  • Weight Range of 75kg to 150kg
  • Age 16 to \<21 at baseline
  • Elevated alanine aminotransferase (ALT) more than twice the upper limit of normal by gender (≥ 44 U/L for girls, ≥ 50 U/L for boys)63 within 3 months prior to screening (used for historic ALT value) OR diagnosis of NAFLD from ultrasound, MRI, or participants with biopsy-proven NASH within 12 months of screening.
  • History of lifestyle modification to treat obesity or NAFLD.
  • Tanner stage \>2
  • Normal fasting glucose (fasting blood glucose \<100 mg/dL) To be obtained at screening visit:
  • Confirmation of obesity;
  • Tanner stage 2,3,4 or 5;
  • Normal fasting glucose tolerance (fasting blood glucose \<100 mg/dL);
  • If Screening ALT is used as inclusion criteria (if \> 2x historic ALT value (historical value obtained clinically within 12 months of screening visit), repeated after 4 weeks \[unable to randomize until completed\]. If the repeat ALT is more than 50% increased or decreased over the screening ALT, a third ALT should be obtained. If a third ALT is not within 50% of the previous value, then the subject is ineligible but may be rescreened at a later date. If ALT is not used:
  • An ultrasound will be done to diagnose NAFLD if the diagnosis has not previously been made by ultrasound, MRI or biopsy.
  • A MRI-derived HFF ≥ 5.5%
  • Willingness to adhere to lifestyle considerations throughout the study

Exclusion criteria

  • ALT \> 250U/L at screening
  • History of significant alcohol intake or current use
  • Impaired fasting glucose (\>100 mg/dL)
  • Diabetes (type 1 or 2)
  • Current or recent (\<6 months prior to enrollment) use of weight loss medication(s)
  • Vitamin E supplementation or use of metformin -washout period 30 days
  • Previous bariatric surgery
  • Prior use of empagliflozin
  • Lower limb infection/ulceration within 3 months of screening
  • Metal or magnetic implants, devices or objects inside of or on the body, which are not MRI compatible
  • Structural and functional urogenital abnormalities, that predispose for urogenital infections
  • Recent initiation (\<3 months prior to enrollment) of anti-hypertensive or lipid medication(s)
  • Major psychiatric disorder
  • Known hypothalamic or pituitary dysfunction
  • Current pregnancy or plans to become pregnant
  • Females unwilling to be tested for pregnancy
  • Females who are sexually active and not protects by an effective method of birth control (e.g. UID or medication or patch) -can re-screen 30 days after getting on birth control
  • Tobacco use
  • Significant liver dysfunction (levels \>5 times the upper limit of normal (ULN)):
  • ALT (ULN = 50 U/L)
  • AST (ULN = 48 U/L)
  • GGT (ULN = 48 U/L)
  • ALP (ULN = 115 U/L)
  • Platelets \< 150,000 cells/mm3
  • Total bilirubin \> 1.3 mg/dL
  • Albumin \<3.2 g/dL
  • Gilbert's Syndrome
  • Any known causes of liver disease (except NAFLD and NASH)
  • Significant renal dysfunction (estimated glomerular filtration rate \[eGFR\] \< 80 mL/min/1.73 m2),
  • Diagnosed monogenic obesity
  • History of cancer
  • Untreated thyroid disorder
  • History of decompensation events (ascites, variceal bleeding, hepatic encephalopathy, or hepatocellular carcinoma)
  • Current or recent (\<6 months prior to enrollment) use of medication(s) associated with weight gain (e.g. atypical anti-psychotics).

Where

  • Chicago, Illinois

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jan 21, 2026 · Source of record for eligibility and locations

📊
1 of 40 participants interested
3% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Chicago

Illinois

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

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

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Non-Alcoholic Fatty Liver Disease Treatment in Chicago?

Join others in Illinois exploring innovative treatment options through clinical research

Non-Alcoholic Fatty Liver Disease Treatment Options in Chicago, Illinois

If you're searching for Non-Alcoholic Fatty Liver Disease treatment in Chicago, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Chicago and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Non-Alcoholic Fatty Liver Disease. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Illinois
Now Enrolling
Up to 40 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Non-Alcoholic Fatty Liver Disease?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Non-Alcoholic Fatty Liver Disease

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Non-Alcoholic Fatty Liver Disease Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06355310. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.