Central Mechanisms That Regulate Glucose Metabolism in Humans

Sponsor
Albert Einstein College of Medicine (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT01028846
Collaborator
National Institutes of Health (NIH) (NIH), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
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Study Details

Study Description

Brief Summary

Type 2 diabetes is a chronic condition that affects the ability of the body to regulate glucose (sugar). When glucose levels are low, the liver can make glucose to increase levels in the body. This important process is called endogenous glucose production (EGP). Previous studies suggest that the central nervous system (CNS), including the brain, helps to coordinate this process by communicating with the liver through potassium channels. Control of EGP can be impaired in people with type 2 diabetes, which may contribute to the high levels of glucose seen in these individuals.

The purpose of this study is to understand how activating these potassium channels in the control centers of the brain with a medication called diazoxide might inhibit the amount of glucose made by the liver. This is particularly important for people with diabetes who have very high production of glucose, which in turn causes hyperglycemia (high levels of sugar in the blood) that leads to diabetes complications.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

In this study, the investigators will study healthy participants through a procedure called a "pancreatic clamp" study. During the clamp procedure, glucose (a sugar) and insulin (a hormone produced in the pancreas that regulates the amount of glucose in the blood) are infused with an intravenous catheter, and blood samples are collected periodically throughout the procedure to measure blood sugar levels and the levels of several hormones that are found in the body and are related to glucose metabolism. Endogenous glucose production (the production of sugar by the liver) will be measured in patients given diazoxide (a medication that activates potassium channels in the brain that may affect glucose production in the liver through brain-liver signaling), compared with when a placebo is given.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
Central Mechanisms That Regulate Glucose Metabolism in Humans
Study Start Date :
May 1, 2011
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Diazoxide

1-2 mg/kg total dose given intravenously during pancreatic clamp study

Drug: Diazoxide
1-2 mg/kg total dose given intravenously

Placebo Comparator: Placebo

Intravenous normal saline during pancreatic clamp study

Drug: Placebo
Intravenous normal saline

Outcome Measures

Primary Outcome Measures

  1. Endogenous Glucose Production (EGP) [Final 60 minutes (t=180-240 minutes) of the pancreatic clamp]

    EGP (a measure of the body's production of sugar) will be measured using analysis of blood samples taken throughout the pancreatic clamp procedure under various treatment conditions (eg, diazoxide or placebo) by monitoring changes in the level of a non-radioactive, naturally occurring form of glucose (sugar).

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy volunteers
Exclusion Criteria:
  • Hyperlipidemia

  • Hypertension

  • Heart disease

  • Cerebrovascular disease

  • Seizures

  • Bleeding disorders

  • Muscle disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Albert Einstein College of Medicine Bronx New York United States 10461

Sponsors and Collaborators

  • Albert Einstein College of Medicine
  • National Institutes of Health (NIH)
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Investigators

  • Principal Investigator: Meredith Hawkins, M.D., M.S., Albert Einstein College of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Albert Einstein College of Medicine
ClinicalTrials.gov Identifier:
NCT01028846
Other Study ID Numbers:
  • 2006-414
  • R01DK069861
First Posted:
Dec 9, 2009
Last Update Posted:
Oct 20, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Albert Einstein College of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 20, 2021