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Role of oxemia in anemic patients with chronic kidney disease.

High Dose Erythropoietin versus desidustat for treatment of anemia in patients of chronic kidney disease having inadequate response to weight based erythropoietin dose: A prospective randomised control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061666
Enrollment
50
Registered
2024-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: N189- Chronic kidney disease, unspecified

Interventions

Intervention1: Tab Desidustat: Oral HIF PHI analogue approved for CKD Anemia patients. Started at dose corresponding to EPO Dosage of 10,000U (125 mg) for 8 weeks. Control Intervention1: Eryhtropoieti

Sponsors

Department Of Nephrology P.G.I.M.E.R. Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Chronic Kidney Disease Patients- Non-Dialysis Dependent CKD Dialysis dependent patients on adequate dialysis i.e.2/3 times a week Ferritin >100 ng/dl T Sat >20%

Exclusion criteria

Exclusion criteria: Haematological Malignancy Hemoglobinopathies Active Bleeding Sepsis or Septic Shock HIV Systemic Immunosupression Therapy Pregnancy / Lactation Severe Hyperparathyroidism ( Intact PTH >9 times normal )

Design outcomes

Primary

MeasureTime frame
Change in Hemoglobin levels from baseline to 8 weeksTimepoint: from baseline to 8 weeks

Secondary

MeasureTime frame
1.Change in iron profile parameters (Serum Iron, Transferrin saturation, Total iron binding capacity, Ferritin) 2. Inflammatory markers (IL1, IL6, Hepcidin, CRP)Timepoint: Baseline and at the end of 2 months

Countries

India

Contacts

Public ContactDr Nikhil Bajiya

Post Graduate Institute of Medical Education and Research, Chandigarh

divyaveer.ss@gmail.com8208839726

Outcome results

None listed

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