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FGF21 and Fructose Challenge in Humans

Beth Israel Lahey Health logo

Beth Israel Lahey Health

Status

Completed

Conditions

Fasting

Treatments

Dietary Supplement: oral carbohydrate challenge

Study type

Interventional

Funder types

Other

Identifiers

NCT02884791
2015P000381

Details and patient eligibility

About

The primary aim of this study is to examine the effect of acute ingestion of fructose on serum FGF21 levels. Subjects in this study will be lean volunteers and individuals with metabolic syndrome.

Full description

Participation in this study involves fasting overnight, drinking a sweet beverage, and several blood draws through an IV line. Each subject may drink up to 10 different sweet beverages, separated by 2 weeks.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria for lean subjects:

  • Men and women ages 18-60
  • BMI 19-25 kg/m2; 19-23 for Asian subjects
  • Stable weight (variation < 3 kg within 6 months of screening visit)
  • Ability to give informed consent
  • Ability to follow verbal and written instructions in English
  • Use of medically approved form of contraception (monophasic oral contraception, intra uterine device, surgical sterilization or 2 combined barrier methods)

Specific exclusion criteria for lean subjects:

  • Fasting blood glucose >100; 2 hr OGTT blood glucose >140
  • Fasting triglycerides >150

Inclusion criteria for metabolic syndrome subjects:

3 or more of the following (based on joint scientific statement by Alberti et al, 2009:

  • Fasting triglycerides >150 mg/dl (or on treatment for elevated triglycerides)
  • HDL cholesterol <40 mg/dl in men or <50 mg/dl in women
  • Blood pressure > 130/85 (or antihypertensive treatment in a subject with history of hypertension)
  • Fasting BG >100
  • Elevated waist circumference ** see below for race and ethnic specifications

Men Women

  • Asian or Central, South or Native American > 90 cm > 80 cm
  • Non-Asian, Non-Latino United States > 102 cm > 88 cm

General Exclusion criteria

  • Type 1 or type 2 diabetes mellitus diagnosed according to American Diabetes Association criteria
  • Coronary heart disease (history of myocardial infarction, unstable angina pectoris, or congestive heart failure)
  • Uncontrolled hypertension (BP > 160/100 mmHg on or off antihypertensive medication)
  • Marijuana or intravenous drug use
  • Recent weight loss (> 3 kg within 6 months of the screening visit)
  • Gastroparesis
  • Inflammatory or irritable bowel disease
  • Malignancy treated with chemotherapy within the past 3 years
  • Depression or psychosis requiring hospitalization
  • Renal insufficiency (creatinine clearance < 40 ml/min)
  • Transaminases > 2x above the normal range
  • Known liver disease
  • Pregnancy within 6 months of the screening visit
  • Lactation
  • Failure to use medically approved contraceptive methods
  • History of surgery for the treatment of obesity (gastric banding, gastric bypass, gastric stapling)
  • Change in dose of thyroid hormone or antithyroidal medication within 3 months of screening visit
  • History of alcohol abuse within the past 5 years
  • Fructose intolerance

Exclusionary medications:

  • Oral steroids
  • Metformin
  • Weight loss medications including nonprescription supplements

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Fasting (Healthy)
Experimental group
Description:
Participation in this study involves fasting overnight, drinking a sweet beverage, and several blood draws through an IV line. Each subject may drink up to10 different sweet beverages, separated by 2 weeks.
Treatment:
Dietary Supplement: oral carbohydrate challenge
Fasting (metabolic syndrome)
Experimental group
Description:
Participation in this study involves fasting overnight, drinking a sweet beverage, and several blood draws through an IV line. Each subject may drink up to10 different sweet beverages, separated by 2 weeks.
Treatment:
Dietary Supplement: oral carbohydrate challenge

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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