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Comparison the effects of Empaglifluzin-linagliptin and Dapaglifluzin-linagliptin on HbA1c ? LDL and Albuminuria in patients with T2DM

Comparison the effects of Empaglifluzin-linagliptin and Dapaglifluzin-linagliptin on HbA1c ? LDL and Albuminuria in patients with T2DM

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221221056889N1
Enrollment
70
Registered
2023-02-23
Start date
2023-03-06
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Type 2 diabetes.

Interventions

First intervention group: empagliflozin-linagliptin drug 5-10 mg daily and one tablet per day for three months. The second intervention group: dapagliflozin-linagliptin 5-10 mg daily, one tablet per d

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: Having type 2 diabetes Hb A1c above 7 and below 11 No acute hospitalization conditions Age between 30 and 75 years Patients with albuminuria Not taking the drug beforehand

Exclusion criteria

Exclusion criteria: Acute hospitalization conditions Pre-medication

Design outcomes

Primary

MeasureTime frame
The main outcome of this study is urine microalbuminuria, which is considered as the main indicator of diabetic nephropathy, LDL and HbA1c. This result is evaluated by spot urine and blood samples at the beginning of the study, three months after the start of the treatment. Timepoint: At the beginning of the study and three months after the start of treatment. Method of measurement: It is evaluated by spot urine and blood samples at the beginning of the study and three months after the start of the treatment.

Secondary

MeasureTime frame
Other outcomes included in the researcher's checklist (attached at the end of the proposal), such as FBS, GFR, and lipid profile, are evaluated by the patient's blood test at the beginning of the study, and after the completion of the treatment period, i.e., three months after the start of the treatment. Timepoint: The beginning of the study and three months after the start of treatment. Method of measurement: By testing the patient's blood.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed seyedi niasar

Arak University of Medical Sciences

sseyedi43@gmail.com+98 86 3836 0000

Outcome results

None listed

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