Trial of Different Dosages' Ge Gen Qin Lian Decoction in the Treatment of Type 2 Diabetes

Not Applicable

• Conditions: Diabetes Mellitus, Type 2; Dose-Response Relationship, Drug
• Interventions: Drug: High Dose GGQL Decoction; Drug: Mild dose GGQL Decoction; Drug: Low dose GGQL Decoction; Drug: Placebo

• Registration Number: NCT01219803
• Lead Sponsor: Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Brief Summary

Ge Gen Qin Lian Decoction are one kind of Chinese prescription, and previous study showed they had antidiabetic effects on the clinical patients and no obvious toxicity was found. The purpose of this study was to evaluate the efficacy and safety of different dosage of Ge Gen Qin Lian Decoction in the treatment of type 2 diabetic patients and explore relationship of the dosage and effect and the safety of 3 dosages of Ge Gen Qin Lian Decoction.

Detailed Description

two hundred and forty primary diabetic patients will be expected to be recruited, which were divided into different groups in a randomized, doubled blind, dose-paralleled-control multi-centre clinical design. The patients were randomly taken with high-dosage(5 times of low-dosage),mild-dosage(3 times of low-dosage), low-dosage,placebo(4.5% of low dosage) by 2 times every day for 12 weeks. Hemoglobin A1c (HbA1c), Fasting plasma glucose (FPG),postprandial 2 hours plasma glucose(2hPG),insulin(0h,1h,2h),syndrome,symptoms,body mass index (BMI),waist circumference (WC) of these groups were measured and analyzed. Some safety indexes such blood and urine and stool routine examination, electrocardiogram (ECG)and liver and kidney function tests were measured and analyzed during the experiment. The treatment period is 12 week.

Study Timeline

• Study Start: 2010-08
• Study First Submitted: 2010-10-12
• Study First Submitted QC: 2010-10-12
• Study First Posted: 2010-10-13
• Status Verified: 2012-05
• Last Update Submitted: 2012-05-05
• Last Update Posted: 2012-05-08
• Primary Completion: 2014-08
• Study Completion: 2014-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

• Clinical diagnosis of type 2 diabetes mellitus
• 30-65 years old
• HbA1c≥7.0%, and FPG>7.0 mmol/L, but <13.9 mmol/L or 2hPG>11.1 mmol/L
• Informed consent has been signed
• Dampness and Heat in Spleen

Exclusion Criteria

• The patients accepted diabetic treatment for more than a month continuously
• The patients were treated by drugs in 3 week before they were given test drugs
• Diabetic ketosis, diabetic ketoacidosis or serious inflammation in a month
• The contractive pressure >160 mmHg or diastolic pressure >100 mmHg
• Pregnant, preparing for pregnancy or breast-feeding women
• Mental patients
• The patients whose ALT or AST are >100U/L,and BUN or Cr are abnormal.
• The patients who have serious heart, lung, liver, kidney and brain or other primary complications
• Allergic persons
• The patients who are attending other clinical trial
• The patients who have serious diabetic complications
• The patients who ever attended this clinical trial
• Alcohol and / or psychoactive substances, drug abuse and dependency
• The person maybe loss for some reason such as work or life condition according to the investigator's judgement
• The lipid-lowering or antihypertensive drug dosage and category which the patients are taking could not be kept stable
• The patients who are eating some drugs or health food which can affect the body weight

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
High dose GGQL Decoction	High Dose GGQL Decoction	-
Mild dose GGQL Decoction	Mild dose GGQL Decoction	-
Low dose GGQL Decoction	Low dose GGQL Decoction	-
Placebo	Placebo	-

Primary Outcome Measures

Name	Time	Method
HbA1c	12 weeks after treatment

Secondary Outcome Measures

Name	Time	Method
Fasting plasma glucose (FPG)、postprandial 2 hours plasma glucose(2hPG)	12 weeks after treatment
blood and urine and stool routine examination, electrocardiogram (ECG)and liver and kidney function tests	12 weeks after treatment
Ins(0h,1h,2h),blood lipids	12 weeks after treatment

Trial Locations

Locations (4)

Beijing Traditional Chinese Medicine Hospital of the Capital University of Medical Sciences; 🇨🇳 Beijing, Beijing, China

China-Japan Friendship Hospital; 🇨🇳 Beijing, Beijing, China

Ji Shui Tan Hospital of Beijing; 🇨🇳 Beijing, Beijing, China

Dongzhimen Hospital Attached to Beijing Traditional Chinese Medicine University; 🇨🇳 Beijing, Beijing, China