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Indian chronic kidney disease (ICKD) study: A prospective, observational cohort study in Indian patients with CKD of moderate severity

Indian chronic kidney disease (ICKD) study: A prospective, observational cohort study in Indian patients with CKD of moderate severity - ICKD study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00003701
Enrollment
5000
Registered
2012-04-13
Start date
2013-01-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Cardiovascular disease N18.9 I51.6

Interventions

Group 1: Patients with CKD will be followed up for at least five years. An interview, physical examination and blood and urine samples will be collected at baseline, and annually thereafter.

Sponsors

Department of Nephrology and Medical Intensive Care, Charité Campus Virchow-Klinikum
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Willing patients with approximately 50% reduction in kidney function (estimated GFR 30-60 ml/min) and/or proteinuria >500 mg/g creatinine or albuminuria >300mg/g creatinine. All patients who fulfill these criteria during the recruitment phase will be informed about the study and requested to sign the consent form. Those patients who provide a written informed consent will be in recruited in the study and followed for a minimum of five years. Any medication therapy is possible and does not affect the inclusion in the ICKD study.

Exclusion criteria

Exclusion criteria: Patients with any organ or bone marrow transplantation; or patients who have received chemotherapy because of any active malignant disease within two years prior to recruitment, or patients with NYHA class III or IV heart failure at baseline, or patients with non-Indian origin will be excluded.

Design outcomes

Primary

MeasureTime frame
The primary renal endpoints include: 1) Requirement of renal replacement therapy (dialysis or transplant) 2) Persistent decline of GFR of at least 50% compared to baseline The primary cardiovascular endpoints include: 1) Non-lethal myocardial infarction (symptomatic or silent) 2) Non-lethal stroke 3) Intervention for peripheral arterial occlusion disease 4) Cardiovascular conditioned death (including sudden cardiac death) 5) Hospitalization caused for cardiovascular reason These endpoints will be recorded at each annual follow-up visit and in-between telephonic interviews during the entire five-year study period. The endpoints will be captured by direct interviews with the patients, hospital discharge summaries, doctor's letters and blood tests.

Secondary

MeasureTime frame
1) General mortality 2) Malignancy 3) Hospitalizations 4) Acute kidney injury

Countries

India

Contacts

Public ContactSeema Baid-Agrawal

Department of Nephrology and Intensive Medical Care, Campus Virchow Klinik, Charite Medical University

seema.baid-agrawal@charite.de+4930 450553373

Outcome results

None listed

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