Actively Recruiting

Phase Not Applicable
Age: 20Years - 55Years
All Genders
Healthy Volunteers
NCT07209202

Fructose Intestinal Gluconeogenesis

Led by Touro University, California · Updated on 2026-03-06

40

Participants Needed

1

Research Sites

221 weeks

Total Duration

On this page

Sponsors

T

Touro University, California

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will test the hypothesis that within a defined range of fructose intake, the ability to convert fructose to glucose (via gluconeogenesis) in the small intestine plays a protective role for the liver, shielding it from the deleterious effects of fructose. We will investigate whether this protective effect of the intestine is impaired in individuals with obesity.

CONDITIONS

Official Title

Fructose Intestinal Gluconeogenesis

Who Can Participate

Age: 20Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • BMI 30 to 38 kg/m2 (obese group) or BMI 19 to 25 kg/m2 (lean group)
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding within the past six months
  • Type 1 or 2 diabetes mellitus (including fasting glucose 65126 mg/dL, HgbA1c 656.5%)
  • History of liver disease or AST and ALT more than twice the upper limit of normal
  • Fasting triglyceride greater than 300 mg/dl
  • Total cholesterol levels above the 95th percentile for age and sex
  • Hemoglobin less than 12.5 g/dL or hematocrit less than three times the hemoglobin value
  • Reported HIV or hepatitis B or C infection
  • History of cancer except basal cell or squamous cell carcinoma
  • Kidney disease stage 3 or higher or currently on dialysis
  • Use of any anti-diabetic or cholesterol-lowering medications in the past six months
  • History of surgical procedures for obesity
  • Change in body weight greater than 5% in the past six months
  • History of conditions affecting insulin sensitivity and lipid metabolism (e.g., polycystic ovary syndrome)
  • History of galactosemia or hereditary fructose intolerance
  • Positive test for fructose malabsorption at screening
  • Known intolerance to acetaminophen

AI-Screening

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Trial Site Locations

Total: 1 location

1

Touro University California

Vallejo, California, United States, 95492

Actively Recruiting

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Research Team

S

Sally Chiu, PhD

CONTACT

L

Lisa Johnson, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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