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Studying the Management of Anaemia in Indian Patients with Chronic Kidney Disease, with and without Dialysis

A Prospective, Multicentre, Longitudinal Disease Registry of Indian Patients with Chronic Kidney Disease, with and without Dialysis, to assess the Clinical management of Anaemia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/01/079069
Enrollment
1000
Registered
2025-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Dr Reddys Laboratories Road No Banjara Hills Hyderabad Telangana India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male and female subjects, aged �18 years. 2. CKD patients (as defined in KDIGO guidelines) with Hb level less than 10g/dl (as per the latest available test report), with/without the need of dialysis and who have newly commenced therapy for anemia, including at least one agent each for stimulating erythropoiesis and iron supplementation, with or without any other agents. 3. Willing to provide inform consent to share the data.

Exclusion criteria

Exclusion criteria: Patients with presence of uncontrolled hypertension, uncontrolled hyperparathyroidism or hypothyroidism or bleeding disorders or acute illness or chronic blood loss or hemoglobinopathy, or malignancy.

Design outcomes

Primary

MeasureTime frame
1. Clinical characteristics in terms of demographics and medical condition of CKD 2. Utilization patterns of various pharmacological classes including but not limited to agents administered to stimulate erythropoiesis, iron supplementation used in management of anaemia in CKD. 3. Assessment of response to various treatment approaches in terms of haematological parameters and quality of life (QoL) based on KDQOL (KDQOL-SFââ??¢ v1.3) 4. Analysis of observed side effects during the management of anaemia in CKD patients with anaemia.Timepoint: Baseline, 3 months, 6 months

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Sagar Katare

Dr. Reddys Laboratories Ltd

sagarkatare@drreddys.com9223772427

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026