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Efficacy and safety research on treatment of type 2 diabetes with vitamin D2 injection

Effect and safety of Vitamin D2 for ameliorate the state of insulin resistance improving insulin resistance in type 2 diabetes mellitus

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056380
Enrollment
Unknown
Registered
2022-02-04
Start date
2022-03-01
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Type 2 diabetes

Interventions

Treatment group:Vitamin D2 injection and standard hypoglycemic therapy
Control group:Standard hypoglycemic therapy and placebo injection

Sponsors

The Second Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 69 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 30 and 69 years, and with the duration of diabetes for 5 to 15 years; 2. No long-term outdoor activities and long-term living plan in tropical areas within 6 months after the start of the clinical trial; 3. Meet the diagnostic criteria of T2DM; 4. Voluntarily participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with ketoacidosis and lactic acidosis in recent 1 month; 2. 25-(OH)D> 20ng/ml; 3. Patients who use drugs that may affect VD metabolism or vitamin D and its analogues; 4. Blood calcium > 11mg/dl (2.75 mmol/L); 5. Vitamin D overdose or poisoning; 6. Patients with history of urinary calculi and sarcoidosis; autoimmune diseases; severe liver function injury; tumor, parathyroid gland, hemocytopenia and other diseases; HIV antibody positive; peripheral neuropathy caused by other causes; other serious acute and chronic diseases or with abnormal laboratory examination, are not allowed to participating in this study; 7. Significant cognitive impairment, mental disorder or physical dysfunction that may affect the completion of research related projects; 8. Alcohol or drug abusers; 9. Allergic to the drugs used in the study protocol; 10. Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
25 hydroxyvitamin D;FPG;FINS;Serum calcium and phosphorus;HbA1C;Fasting C-peptide;

Countries

China

Contacts

Public ContactHu Ji

The Second Affiliated Hospital of Soochow University

whogee@gmail.com+86 13771780309

Outcome results

None listed

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