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Type 2 diabetes changing insulin regimen to non-insulin regimen to reach target of glucose: a retrospective case records based study

Type 2 diabetes changing insulin regimen to non-insulin regimen to reach target of glucose: a retrospective case records based study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ORC-15007634
Enrollment
Unknown
Registered
2015-12-17
Start date
2016-01-01
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

Type 2 diabetes mellitus

Interventions

Case series:Nil

Sponsors

Shandong Provincial Qianfoshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. diagnosed as T2DM based on the diagnostic standards issued by WHO in 1999; 2. had been treated with insulin based on the Chinese type 2 diabetes guidelines without well-controlled plasma glucose but fasting blood glucose, postprandial blood glucose, and glycosylated hemoglobin A1c reached target after alternation to non-insulin regimen; 3. had gotten advises from professional endocrinologist for more than 3 times (including diet, exercise, and recommended usage of insulin); 4. the information conserved integrated and the main outcomes were provide by Shandong Provincial Qianfoshan Hospital.

Exclusion criteria

Exclusion criteria: 1. diagnosed as T1DM or other kinds of diabetes mellitus based on the diagnostic standards issued by WHO in 1999; 2. diagnosed as latent autoimmune diabetes in adult; 3. in pregnancy or lactation; 4. used insulin out of the specification, continually used insulin or used both insulin and non-insulin drugs; 5. had not visited licensed medical facilities before; 6. lost information or the main outcomes were provided by other hospitals; 7. lost in the follow up period; 8. complicated with acute stress reaction or acute complications; 9. had explicit alternation of life-style after therapy changing.

Design outcomes

Primary

MeasureTime frame
fasting blood-glucose;postprandial blood glucose;haemoglobin A1c;

Secondary

MeasureTime frame
incidence of hypoglycemia;incidence of diabetic keto-acidosis;body weight;

Countries

China

Contacts

Public ContactLiao Lin
liaolin009@sina.com+86 0531-82963647

Outcome results

None listed

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