Skip to main content
OpenTrials
Completed

NCT Number: NCT01940302

Dietary Supplement of LEHEL for the Patients With Type 2 Diabetes

Due to metabolic disorders and dietary restrictions, patients with diabetes may have different degrees of malnutrition. The primary objective of this study is to investigate whether supplementation of LEHEL, a multi-nutrients supplement, is capable to improve metabolic parameters in patients with type 2 diabetes.

Completed

Looking for future studies?

Notify Me

Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Shaoguan University

Shaoguan, Guangdong, 512005, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject is diagnosed with type 2 diabetes mellitus according to the Chinese type 2 diabetes prevention guide 2010, diagnostic criteria are as follows:

(1) Diabetes symptoms(polydipsia、polyphagia, polyuria, weight loss、skin itching、blurred vision and other acute metabolic network disorder that caused by high blood sugar)combined with random blood sugar ≥11.1 OR, (2) fasting plasma glucose (FPG) ≥7.0 OR, (3) 2 h blood sugar after oral glucose tolerance test (OGTT) ≥11.1;

  • Subject is between 18 and 75 years of age, inclusive.
  • Subject's BMI is >18.5 kg/m2 and <35 kg/m2.
  • If on a chronic medication such as anti-hypertensive, lipid-lowering, thyroid medication or hormone therapy, subject has been on constant dosage for at least two months prior to screening visit.

Exclusion criteria

  • Subject that is diagnosed as type 1 diabetes, gestational diabetes and other kinds of diabetes expect type 2.
  • Subject that use exogenous insulin for glucose control.
  • Subject that has a history of diabetic ketoacidosis.
  • Subject that has mental disorder, cancer, cirrhosis, renal disease and hepatic disease.
  • Subject that has had a significant cardiovascular event less than six months prior to screening visit or has history of congestive heart failure.
  • Subject that has had operation less than six months prior to screening visit.
  • Subject that has taken/is currently taking any dietary supplements or medications that could profoundly affect blood glucose during the past one month prior to screening visit.
  • Subject is known to be allergic or intolerant to any ingredient found in the study product.

Treatment and study plan

LEHEL multi-nutrients supplement

Dietary Supplement

The primary objective of this study is to evaluate the effect of a diet program including LEHEL multi-nutrients supplement as breakfast replacement on metabolic control after 12-week intervention in subjects with type 2 diabetes.

Primary outcomes

  1. Metabolic Control

    Time frame: Twelve weeks

    Hemoglobin A1c (HbA1c) and lipids (Cholesterol, HDL-cholesterol, Triglycerides) at study entry and 12 weeks after dietary intervention

Sponsors and collaborators

Lead sponsor

Shaoguan University

Other

Collaborators

  • Sun Yat-sen University

Registry information

Official study title

Metabolic Control Before and After Supplementation With LEHEL in Patients With Type 2 Diabetes

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
Sep 12, 2013
Registry last updated
May 12, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.