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Efficacy and safety of dapagliflozin and acarbose in type 1 diabetes mellitus

Efficacy and safety of dapagliflozin and acarbose in type 1 diabetes mellitus

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019724
Enrollment
Unknown
Registered
2018-11-25
Start date
2018-11-24
Completion date
Unknown
Last updated
2018-12-04

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

Conditions

Type 1 diabetes mellitus

Interventions

Group 2:dapagliflozin 10mg qd
Group 1:Acarbose 50mg tid

Sponsors

Department of Endocrinology, the First Affiliated Hospital of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Diagnosed type 1 diabetes, age 18-60 years old, using insulin to control blood glucose

Exclusion criteria

Exclusion criteria: (1) pregnant or planned pregnancy, breast-feeding; (2) renal insufficiency (eGFR < 60ml/min/1.73m2); (3) diabetes ketosis or ketoacidosis occurred in the last 3 months; (4) urinary tract infection or genital infection; (5) Alpha-Glucosidase Inhibitor or SGLT-2 Inhibitor had been used in the last three months of treatment. Those who were previously known to be intolerable to Alpha-Glucosidase Inhibit or SGLT-2 Inhibitor; (6) Severe liver dysfunction or other important organ dysfunction (such as cardiac insufficiency, chronic respiratory failure, etc.) and severe anemia; (7) Those who had acute myocardial infarction, cerebrovascular accident and severe infection within one month before admission to the group; (8) Using glucocorticoids and other drugs that affect blood glucose; (9) those who underwent surgery during the planned study period; (10) Allergies to medical adhesives or alcohol for disinfection; (11) Local skin damage, scarring, infection, edema or other skin lesions on the application site; (12) Patient with a history of mental illness or other conditions who can not wear sensors as required; (13) Those who fail to follow the research plan and carry out research tasks.

Design outcomes

Primary

MeasureTime frame
mean amplitude of glycemic excursions;

Countries

China

Contacts

Public ContactShaoda Lin

The First Affiliated Hospital of Shantou University Medical College

linshaoda@126.com+86 0754-88905428

Outcome results

None listed

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