Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With Type 2 Diabetes

Completed · Phase 2/Phase 3

Conditions studied: Type 2 Diabetes

In brief

The purpose of the study was to evaluate the effect of an herbal extract on postprandial glycemia following a meal.

Key facts

Study ID

NCT00499148

Run by

Abbott Nutrition

People needed

59

Starts

2006-08-01

Expected to finish

2007-10-01

Last updated by the study team

2010-07-30

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• type 2 diabetes
• Between 18 and 75 years of age
• Male or non-pregnant, non-lactating female, at least 6 weeks postpartum
• If of childbearing potential, is practicing birth control
• BMI is more than or equal to 18kg/m2 and less than or equal to 35kg/m2
• If on anti-hyperglycemic, anti-hypertensive, lipid-lowering, or thyroid medications or hormone therapy, has been on constant dosage for at least 3 months prior to screening visit

You may not qualify if…

• Uses insulin for glucose control or has type 1 diabetes
• History of diabetic ketoacidosis.
• Current infection; surgery or corticosteroid treatment in the last 3 months or antibiotics in the last 3 weeks.
• Active malignancy
• Significant cardiovascular event less than or equal to 6 months prior to screening visit or history of congestive heart failure
• End state organ failure or status post organ transplant
• History of renal disease
• Current hepatic disease
• History of severe gastroparesis
• Has a chronic, contagious, infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV
• Currently taking herbals, dietary supplements, or medications, other than anti-hyperglycemic medications, during the past 4 weeks that could profoundly affect blood glucose
• Clotting or bleeding disorders
• Allergic or intolerant to any ingredient found in the study products

Where it is running

• Radiant Research — Edina, Minnesota, United States
• Radiant Research — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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