Metformin Hydrochloride and Empagliflozin Tablets in the Treatment of Type 2 Diabetes
- Sponsor
- Sun Yat-sen University
- Study ID
- NCT07003191
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Metformin Hydrochloride and Empagliflozin tables (Fixed-Dose Combination) — DRUGFirst-time treatment with Metformin Hydrochloride and Empagliflozin Tablets (metformin 500mg and empagliflozin 5mg per table) for at least 6 months
Study Details
The main objective of this study is to evaluate the efficacy and safety of Metformin Hydrochloride and Empagliflozin Tablets in the treatment of type 2 diabetes in real-world clinical settings. A total of 2,600 type 2 diabetes patients were included in the study. The study observed the clinical glycemic control rate and adverse events over a period of at least 6 months from the prescription date to the end of continuous clinical follow-up.
Key Dates
- Start date
- Aug 2, 2023
- Status verified
- May 2025
- Primary completion
- Dec 31, 2025
- Completion
- Dec 31, 2025
Study Design
- Enrollment
- 2,600 participants (estimated)
Primary Outcome Measure
6-month clinical glycemic control rate [ Time Frame: 6 months ]
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