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Assessment of effectiveness of Empagliflozin in the management of Anemia in diabetes patients

Assessment of Effectiveness of Empagliflozin in the Management of Anemia in Type 2 Diabetes Patients with Early Stage of Chronic Kidney Disease- A Prospective Randomised COntrol Study - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063292
Enrollment
56
Registered
2024-02-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: E112- Type 2 diabetes mellitus with kidney complications

Interventions

Intervention1: Empagliflozin: 25mg tablet orally given once daily for a duration of 3 months Control Intervention1: Standard treatment for type 2 diabetes mellitus.: standard treatment prescribed for

Sponsors

SRM Insitute of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Estimated glomerular filtration rate 45 to 90 ml per minute . Diabetic patients HbA1C greater than 6.5 percent Patients with haemoglobin less than 13.0 g per dL in males. Haemoglobin less than 12.0 g per dL in females.

Exclusion criteria

Exclusion criteria: End Stage Renal Disease patients Stage 4 Patients with hereditary iron metabolism disorders. Patients with Type 1 Diabetes mellitus. Patients with pre-existing Urinary tract or Genital infections and patients who develop this complication during the study. Patient with pyelonephritis. Patients already taking diuretics. Pregnant and Lactating women. Treatment with any other investigational drug within the previous 30 days of inclusion in the study. Any therapy or condition that would pose a risk to the patient or make it difficult to comply with study requirements. Difficulty in Socio Culture Communication.

Design outcomes

Primary

MeasureTime frame
Serum erythropoietin, ferritin and transferrin saturation will be assessed at baseline and after 3months.Timepoint: 3 months

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactArunshankar P

SRM Institute of Science and Technology

jagadeem1@srmist.edu.in7449277556

Outcome results

None listed

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