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NCT05715307Completed

Chinese Endocrinologists Health Education Study

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to conduct a prospective, multicenter, cluster randomized control study, to evaluate the improvement for T2DM treatment ability in Chinese endocrinologists after 1-week intensive experiential diabetes management training in Ruijin Hospital.

Status (registry)
Completed
Study type
Interventional
Enrollment
2017 (actual)
First submitted
5 Jan 2023
Start date
13 Feb 2023
Primary completion date
25 Oct 2024
Lead sponsor
Shanghai Jiao Tong University School of Medicine
NCT number
NCT05715307

What you commit to

  • Study type: Interventional
  • Participants enrolled: 2017
  • From 13 Feb 2023 to the primary completion date, 25 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 1\. Subjects with type 1 diabetes, single gene mutation diabetes, diabetes due to pancreatic injury or other secondary diabetes (such as Cushing's syndrome, thyroid dysfunction or acromegaly, etc.);
  • 4\. Subjects who were or are using insulin to control diabetes in the past 3 months;
  • 5\. History of drug abuse;
  • 6\. History of sexually transmitted disease (such as syphilis, and HIV infection \[AIDS\], etc.) or in the active phase of infectious disease (such as viral hepatitis, and tuberculosis, etc.);
  • 9\. Any condition that in the judgement of the investigator precludes participation.
    • Details please see the study protocol.

Lab values

  • 2\. Subjects with serious cardiovascular diseases, such as congenital heart disease, rheumatic heart disease, hypertrophic or dilated cardiomyopathy and chronic congestive heart failure (NYHA III-IV); acute myocarditis within 12 months; severe liver and kidney dysfunction (eGFR\<60mL/min/1.73m2); mental disorder, etc.

Other

  • 3\. Subjects with acute diabetic complications in the past 3 months;
  • 7\. Subjects who are pregnant or in lactation;
  • 8\. Participation in other clinical trials;

Who the study is looking for

  • 1\. Subjects with type 2 diabetes mellitus;
  • 2\. First visit to MMC;
  • 3\. Age 40-65 years;
  • 4\. 24.0 \< BMI ≤ 35.0 kg/m2;
  • 5\. Subjects with screening HbA1c ≥ 7.5% and ≤ 10.0%, and the fasting blood glucose ≥ 8.0 mmol/l and \< 13.3 mmol/l;
  • 6\. Duration of diabetes less than 10 years;
  • 7\. Subjects with poorly controlled blood glucose only by 1-2 kinds of non-insulin hypoglycemic drugs for at least 2 months;
  • 8\. Subjects understand the nature, significance, potential benefits, inconvenience, and risks of the study before it starts, and fully understand the study procedures and voluntarily sign the informed consent form.

Age in the registry: 40 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.