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Effectiveness of supplementation of Nefrosave? in Chronic Kidney Disease

Effectiveness and tolerability of N-acetylcysteine and taurine in patients of chronic kidney disease with type 2 diabetes mellitus and/or hypertension: A real-world, retrospective, comparative study from electronic medical records - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/093387
Enrollment
450
Registered
2025-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Fourrts India Laboratories Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or female patients more than and equal to 18 years of age 2. Diagnosis of stage 1, stage 2, or stage 3 chronic kidney disease (CKD) as per the National Kidney Foundation-Kidney Disease Outcomes Quality Initiative (NKF-KDOQI) 3. Diagnosis of type 2 diabetes mellitus (T2DM) and/or hypertension (HTN) by the treating cardiologist 4. Patients on standard of care with or without N-acetylcysteine (NAC; 150 mg) and taurine (500 mg), as prescribed by the treating cardiologist 5. Patients with available data on uACR, serum creatinine, and eGFR as part of routine clinical practice at least at baseline and after 12+2 weeks of treatment

Exclusion criteria

Exclusion criteria: 1. Incomplete medical records with respect to the required study parameters

Design outcomes

Secondary

MeasureTime frame
Change in eGFR from baseline to 12+2 weeks of treatmentTimepoint: Baseline, 12?2 weeks;Proportion of patients with adverse events (AEs) and serious AEs (SAEs)Timepoint: Baseline to 12?2 weeks of treatment

Primary

MeasureTime frame
1. Change in urinary albumin to creatinine ratio (uACR) from baseline to 12?2 weeks of treatment 2. Change in serum creatinine levels from baseline to 12?2 weeks of treatmentTimepoint: 1. Baseline to 12?2 weeks of treatment 2. Baseline to 12?2 weeks of treatment

Countries

India

Contacts

Public ContactDr Monjori Mitra

Medclin Research Pvt Ltd

monjori.mitra@medclinsearch.com9831075734

Outcome results

None listed

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