Effects of Tianqi Capsule on Glucose Variability in Patients With Type 2 Diabetes.

Chinese Academy of Medical Sciences & Peking Union Medical College

Status: Unknown

Conditions: Type 2 Diabetes Mellitus

Treatments: Drug: Tianqi capsule; Drug: placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT02617732

PUMCH-TCM-TQGV-01

Details and patient eligibility

About

The purpose of this study is to evaluate the effects and safety of Tianqi Capsule on glucose variability in patients with type 2 diabetes by continuous blood glucose monitoring system.

Full description

Diabetes has become a threat to human health and an independent risk factor to macrovascular and microvascular diseases. Large prospective clinical studies have shown a strong relationship between time-averaged mean levels of glycemia as measured by HbA1c and diabetes complications. However, in recent years several pieces of evidence indicated that glucose variability may also contribute to the development of diabetes complications. Thus, glucose variability may become a new target in treatment of diabetes. Traditional Chinese medicine，a kind of multitargeted compound, may contribute to maintaining blood glucose homeostasis in diabetes.

Tianqi capsule(Chinese herbs extract) is a Chinese patent medicine approved to treat T2DM in China. Previous clinical studies have shown that Tianqi capsule could lower blood glucose measured by HbA1c. What's more, Tianqi capsule has also been proved to improve the glycometabolism and lipid metabolism in T2DM and IGT.

This research adopts a randomized, open, parallel double blind, placebo controlled clinical method. The patients, meeting eligibility criteria, are divided into experimental group and placebo group and treated for 12 weeks . A main outcome，glucose variability is detected by continuous blood glucose monitoring system which could obtain continuous and comprehensive blood glucose by "glucose sensor". The influence of Tianqi capsule on glucose variability in type 2 diabetes will be evaluated.

Enrollment: 100 estimated patients

Sex: All

Ages: 20 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

• 18.5kg/m2≤BMI≤35.0 kg/m2;
• meet type 2 diabetes mellitus diagnostic criteria published by 1999 WHO;
• with blood variability, defined as standard deviation of blood glucose more than 3.5mmol／L within 2 days by self-monitoring of blood glucose（SMBG）(more than 5 times per day)
• diabetic duration more than 1 year; in stable condition for more than 4 weeks with unchanged lifestyle and other drugs intervention; （permit taking metformin or sulphonylureas which dosage is unchanged during study period ）
• HbA1c≤10％;
• signed the informed consent form.

Exclusion Criteria:

• have acute diabetes complications （e.g. diabetic ketoacidosis，diabetic hyperosmolar coma,diabetic lactic acidosis,Hypoglycemic coma）
• have severe chronic diabetes complications(e.g. diabetic retinopathy stage 4~6,severe diabetic nephropathy needs dialysis and so on）
• have gastrointestinal disease which have serious influence on digestive function and disorder of absorption
• have other endocrine disease (hyperthyroidism,acromegaly,Cushing's syndrome and so on.)
• have severe heart disease(such as acute myocardium infarction, unstable angina,heart failure NYHA functional classification III or IV）
• have moderate or severe liver function abnormality(ALT,TBil or AST> double upper limit )
• have moderate and severe renal function abnormality(eGFR < 50ml／min)
• blood leukocyte <4.0×10^9/L; blood thrombocyte<90×10^9/L
• taking drugs affecting glucose metabolism,such as glucocorticoid
• have other serious illness which considered to exacerbate and be life-threaten during fellow up period;
• have evidence of mental disorders;
• alcoholics and drug abuse
• females who were pregnant, lactating, planning for pregnancy, or sexually active but with no contraceptive measures;
• have participated in clinical trials within 3 months before;
• other conditions researchers thought to unable to evaluate the curative effect and finish the study.
• allergic to the ingredients of herbs contained in Tianqi capsule

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

100 participants in 2 patient groups, including a placebo group

Tianqi capsule

Experimental group

Description:

a Chinese patent medicine extracted form more than10 kinds of herbs, which was approved to treat type 2 diabetes by CDFA in 2002.

Treatment:

Drug: Tianqi capsule

placebo

Placebo Comparator group

Description:

a capsule looks the same as Tianqi capsule, containing starch and other edible compositions.

Treatment:

Drug: placebo