ClinicalTrials.Veeva

Menu

The Long-term Effect of Tianqi Capsule Interventions to Prevent Diabetes in the REDUCES Study: a 8-year Follow-up Study

G

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Status

Unknown

Conditions

Impaired Glucose Tolerance
Type 2 Diabetes Mellitus

Treatments

Other: no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02848053
REDUCES-01

Details and patient eligibility

About

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.

Full 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.

Enrollment

420 estimated patients

Sex

All

Ages

25 to 70 years old

Volunteers

No Healthy Volunteers

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.

Trial design

420 participants in 2 patient groups

Tianqi group
Description:
used Tianqi Capsule in the REDUCES study
Treatment:
Other: no intervention
Placebo group
Description:
used placebo in the REDUCES study
Treatment:
Other: no intervention

Trial contacts and locations

0

Loading...

Central trial contact

Fengmei Lian, PHD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems