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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ChiCTR |
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Last refreshed on:
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18 April 2017 |
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Main ID: |
ChiCTR-IPR-15006366 |
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Date of registration:
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2015-05-05 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Improve the Outcome of Glycemic Control by Enhance the Diabetic Patients' Awareness of Risk: A Randomized Double-blind Controlled Trial
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Scientific title:
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Improve the Outcome of Glycemic Control by Enhance the Diabetic Patients' Awareness of Risk: A Randomized Double-blind Controlled Trial |
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Date of first enrolment:
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2015-04-27 |
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Target sample size:
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1:40;2:40; |
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Recruitment status: |
Recruiting |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=10925 |
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Study type:
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Interventional study |
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Study design:
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Randomized parallel controlled trial
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Phase:
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Pilot study
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Countries of recruitment
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China
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Contacts
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Name:
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Yingying Xiang
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Address:
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22 Qi Xiangtai Rd, Tianjin, China
300070
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Telephone:
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+86 13612043240 |
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Email:
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lovexiangyingying@163.com |
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Affiliation:
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Tianjin Medical University |
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Name:
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Zhongming Wu
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Address:
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22 Qi Xiangtai Rd, Tianjin, China
300070
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Telephone:
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+86 13672093136 |
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Email:
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wuzhongming@tmu.edu.cn |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. Outpatients in line with diagnostic criteria for type 2 diabetes;
2. The duration of diabetes is over 1 year,whitout obvious diabetes complications;
3. Combined with diet, exercise and the current regimen, blood glucose is still poorly controlled,HbA1C>=7.5%;
4. Age 30 to 70 years.
Exclusion criteria: 1. Type 1 diabetes or secondary diabetes;
2. Gestational diabetes, lactational diabetes and diabetes planning to be pregnant;
3. With any major psychiatric disorder;
4. Alcohol or psychoactive substance abusers and addicts;
5. With resistant hypertension;
6. According to the judgment of researchers, it will reduce the possibility to participate the study or make the participating more complex, for example, change the work or living environment frequently.
Age minimum:
30
Age maximum:
70
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Type 2 Diabetes Mellitus
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Intervention(s)
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1:Intensive Education;2:Gneral Education;
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Primary Outcome(s)
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HbA1C;Fasting blood glucose;2 hour postprandial blood glucose;SDSCA;
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Secondary Outcome(s)
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Body weight;serum lipid;
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Source(s) of Monetary Support
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The patients will pay for the costs of the drugs and tests demanded by this clinical trial
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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