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Comparing efficacy of oral desidustat versus injectable eryhtropoetin in treatment of anemia in kidney disease patients

Assessing the differential impact of Desidustat on Reticulocyte iron indices over traditional erythropoietin in Chronic Kidney Disease (CKD) patients irrespective of Iron status - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/09/093963
Enrollment
50
Registered
2025-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: D631- Anemia in chronic kidney disease

Interventions

Intervention1: Hypoxia Inducible Factor- Prolyl Hydroxylase Inhibitors: Oral drug that treats anaemia in Chronic Kidney Disease by mimicking exposure to hypoxia, stimulating endogenous erythropoietin

Sponsors

Gunn Goel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with CKD stage 3, 4,5 (estimated Glomerular Filtration Rate below 60) with stable kidney function in past 3 months assessed by eGFR calculation with anemia (Hb less than 10 g per dL) who have given the consent to participate in the study shall be included in the study

Exclusion criteria

Exclusion criteria: 1.Patients already on Desidustat or EPO for treatment of anaemia prior to screening 2.Patients with a history of or active bleeding 3.Post kidney allograft transplantation 4.Pregnant or expectants 5.Patients on oral or parenteral Iron therapy 6.Patients with vitamin B12, Folate deficiency 7.Patients with underlying malignancy 8.Other causes of anaemia like Hemoglobinopathies, Autoimmune haemolytic anaemia, Hypersplenism, Bone marrow disorders etc 9.Patients with HIV 10.Patients with Cirrhosis 11.ADPKD patients

Design outcomes

Primary

MeasureTime frame
1.To detect change in reticulocyte indices from baseline after a short-term treatment with Desidustat and Standard EPO therapy. 2.To confirm role of Desidustat in mobilising iron stores.Timepoint: Monthly basis for 2 months

Secondary

MeasureTime frame
To study differential impact of iron status on efficacy of Desidustat versus EPO therapy.Timepoint: Monthly basis for 2 months

Countries

India

Contacts

Public ContactDr Saurabh Nayak

All India Institute of Medical Sciences Bathinda

saurabhnayak2012@gmail.com7506150224

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026