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The effect of metformin on serum endogenous soluble RAGE level in Subjects with Impair Glucose Tolerant

The effect of metformin on serum endogenous soluble RAGE level in Subjects with Impair Glucose Tolerant

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004274
Enrollment
Unknown
Registered
2014-02-17
Start date
2014-03-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impair Glucose Tolerant

Interventions

treatment group:Metformin cloridrate
Control:Education of diet and movement

Sponsors

the First Affiliated Hospital of NanChang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Understanding and willing to participate in the test before the signing of the subjects informed consent; 2. Aged 30 to 64 years; 3. According to the WHO standard, the subjects should be diagnosed as IGT; 4. No taking any medicine affecting blood glucose; 5. BMI 20 to 35 kg/m2; 6. HbA1c 6.0 to 6.4%; 7. The subjects were able to and willing to self monitoring of blood glucose.

Exclusion criteria

Exclusion criteria: 1. Hepatic and renal function damage, 2.5 times larger than the upper limit of the normal value of ALT; 1.5 times larger than the upper limit of the normal value of serum creatinine; 2. A history of drug abuse and alcohol dependence history in the past 5 years; 3. Treatment with systemic corticosteroids within 2 months before the 3 screening; 4. The clinical significance of the activity, the (past 12 months) of cardiovascular disease subjects (including a history of myocardial infarction (MI), ECG was shown to arrhythmia or conduction block, unstable angina, or decompensated heart failure (New York Heart Association [NYHA] class III and class IV); 5. The known hypersensitivity to test the pharmaceutical or related products; 6.The pregnancy, breastfeeding or interested in pregnancy, or judgment for not using adequate contraception (adequate contraception is the IUD, oral contraceptives and impede measures); 7. Any other decision by the investigator obvious or combined diseases: such as endocrine, heart, nerve, tumor and other diseases, other pancreatic disease or, painful neuropathy; 8.Blood pressure can not be controled after treatment / without treatment of severe hypertension (defined as systolic pressure = 180mmHg and / or DBP = 100mmHg); 9. He or she had participated in other clinical study of drugs or devices in the past 3 months; 10. Mental disorders, unwilling or language barriers, difficulty understanding, cooperation and the use of blood glucose meter maker.

Design outcomes

Primary

MeasureTime frame
esRAGE;

Secondary

MeasureTime frame
hsCRP;TNF-a;

Countries

China

Contacts

Public ContactXU Jixiong

the First Affiliated Hospital of NanChang University

xujixiong@163.com+86 13307086069

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026