Trials / Completed
CompletedNCT03770052
Glucose-Lowering Effects and Safety of Adding 0.25 or 0.5 mg Duvie
A Double Blind, Randomized, Investigator Initiated Study on Glucose-Lowering Effects and Safety of Adding 0.25 or 0.5 mg Duvie (Lobeglitazone) in Patients With Type 2 Diabetes With Inadequate Control on Metformin and DPP-4 Inhibitor Therapy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 159 (actual)
- Sponsor
- Pusan National University Hospital · Academic / Other
- Sex
- All
- Age
- 19 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Glucose-Lowering Effects and Safety of Adding 0.25 or 0.5 mg Duvie
Detailed description
This study is a double blind, randomized, investigator initiated study on glucose-lowering effects and Safety of Adding 0.25 or 0.5 mg Duvie (Lobeglitazone) in Patients With Type 2 Diabetes With Inadequate Control on Metformin and DPP-4 Inhibitor Therapy. The primary aim of the study is to compared changes of HbA1c between 0.25mg robeblitazone add-on group and 0.5mg robeglitazone add-on group.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | duvie | take the intervention drug once daily according to the randomized groups |
Timeline
- Start date
- 2018-10-24
- Primary completion
- 2021-08-19
- Completion
- 2021-09-13
- First posted
- 2018-12-10
- Last updated
- 2022-01-20
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03770052. Inclusion in this directory is not an endorsement.