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Insulin Variance Throughout the Day

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Pennington Biomedical Research Center

Status

Completed

Conditions

Insulin Sensitivity

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01546545
PBRC 11021

Details and patient eligibility

About

This study is designed to determine whether the sensitivity of a participant's insulin varies from the morning to the evening.

Full description

Study visit 1: about 16 hours - The participant will arrive to the visit fasting.

The participant will have an oral glucose tolerance test which takes about 3 ½ hours.

An IV line will be placed in the participant's arm vein for blood draw purposes and will remain there throughout the testing. A blood sample will be drawn 15 minutes and just before the participant will drink a sugar solution consisting of 75 grams of glucose. Blood will be drawn at specific times after the participant consumes the drink.

The participant will have a second oral glucose tolerance test which takes about 3 ½ hours. An IV line will be placed in the participant's arm vein for blood draw purposes and will remain there throughout the testing. A blood sample will be drawn 15 minutes and just before the participant drinks a sugar solution. Blood will be drawn at specific times after the participant consumes the drink.

Enrollment

11 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Are a healthy male or female
  • Have a fasting blood sugar that is between normal and diabetes.
  • Are between 18 and 70 years of age, inclusive.

Exclusion criteria

  • Are pregnant or breast-feeding a child
  • Take a medication for diabetes
  • Take a medication like cortisone that can change your blood sugar.
  • Take a medication chronically that has not been at a stable dose for at least 1 month
  • Take medication for psychosis that is known to change timing in the day - night cycle

Trial design

11 participants in 1 patient group

Insulin Sensitivity in Pre-Diabetic Population
Description:
Healthy participants between the age of 18 and 70 years with fasting blood sugar that is between normal and diabetes.

Trial contacts and locations

1

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Central trial contact

Tance Sonnier, BS; Jeffrey Gimble, MD, PhD

Data sourced from clinicaltrials.gov

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