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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02848053
Other study ID # REDUCES-01
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 21, 2016
Last updated October 3, 2016
Start date August 2016
Est. completion date November 2016

Study information

Verified date October 2016
Source Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Contact Fengmei Lian, PHD
Phone 0086-010-88001402
Email lfm565@sohu.com
Is FDA regulated No
Health authority State Administration of Traditional Chinese Medicine: China
Study type Observational

Clinical Trial Summary

Objectives: This study is aimed to assess whether Tianqi Capsule interventions have a long-term effect on the risk of diabetes and provide evidence that early intervention by traditional Chinese medicine could delay the progression from impaired glucose tolerance to diabetes.

Study contents: 1.420 participants were followed up for 8 years to assess the long-term effect of Tianqi Capsule. Phone-call followed up was applied to investigate the status of impaired glucose tolerance and orthoglycemic survivors until the end of REDUCES study. 2.To participants that determined the status of glucose metabolism, a variety of ways were used to find the evidence of diagnosis of glucose metabolic status, such as glycemia laboratory sheets from normal hospitals, medical records, the use of antidiabetic drugs or insulin injection, etc. 3. To participants that undiagnosed the status of glucose metabolism, oral glucose tolerance test, blood pressure, weight and blood biochemical analysis were performed to assess the state of glucose metabolism. 4. Questionnaires were given to all the participants to investigate their condition of treatment, diet, exercise and other lifestyle.


Description:

Study design: Perspective study Study drug: Tianqi CapsuleInclusion criteria: 1. Subjects have participated in the REDUCES study before; 2. Informed consent forms were needed to participants performed to blood test; 3. Laboratory sheets could be voluntary acquirement by participants that determined the status of glucose metabolism; 4.Subjects were not disabled, and could take care of themselves. 5. Subjects did not suffer the infectious disease.

Exclusion criteria: 1. Subjects did not participate the REDUCES study; 2. Subjects suffered serious mental illness; 3. Subjects suffered severe mental or cognitive impairment; 4. Subjects had a history of drug or alcohol dependence; 5. Subjects have participated in other drug clinical trials in the past 1 month.

Main outcome index: Incidence of diabetes. Secondary outcome index: Body mass index, fasting blood-glucose, postprandial blood sugar, blood lipids, blood pressure.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 420
Est. completion date November 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 70 Years
Eligibility Inclusion Criteria:

- Subjects have participated in the REDUCES study before;

- Informed consent forms were needed to participants performed to blood test;

- Laboratory sheets could be voluntary acquirement by participants that determined the status of glucose metabolism;

- Subjects were not disabled, and could take care of themselves. 5. Subjects did not suffer the infectious disease.

Exclusion Criteria:

- Subjects did not participate the REDUCES study;

- Subjects suffered serious mental illness;

- Subjects suffered severe mental or cognitive impairment;

- Subjects had a history of drug or alcohol dependence;

- Subjects have participated in other drug clinical trials in the past 1 month.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Intervention

Other:
no intervention


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Guang'anmen Hospital of China Academy of Chinese Medical Sciences Hubei College of Traditional Chinese Medicine

References & Publications (1)

Lian F, Li G, Chen X, Wang X, Piao C, Wang J, Hong Y, Ba Z, Wu S, Zhou X, Lang J, Liu Y, Zhang R, Hao J, Zhu Z, Li H, Fang Liu H, Cao A, Yan Z, An Y, Bai Y, Wang Q, Zhen Z, Yu C, Wang CZ, Yuan CS, Tong X. Chinese herbal medicine Tianqi reduces progression — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of diabetes 0 week No
Secondary Number of participants with abnormal body mass index values (in kg/m^2) 0 week No
Secondary Number of participants with abnormal Triglycerides values (in mmol/L) 0 week No
Secondary Number of participants with abnormal Cholesterol values (in mmol/L) 0 week No
Secondary Number of participants with abnormal Low density lipoprotein values (in mmol/L) 0 week No
Secondary Number of participants with abnormal High density lipoprotein values (in mmol/L) 0 week No
Secondary Number of participants with abnormal Systolic Blood Pressure values (in mmHg) 0 week No
Secondary Number of participants with abnormal Diastolic Blood Pressure values (in mmHg) 0 week No
Secondary Number of participants with abnormal blood glucose values (in mmol/L) 0 week No
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