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Dual RAAS blockage in primary glomerular diseases

Randomized Control Trial to study the safety and efficacy of dual blockade of Renin Angiotensin Aldosterone System (RAAS) in Primary Glomerular diseases.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052593
Enrollment
100
Registered
2023-05-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: N003- Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis Health Condition 2: N005- Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis Health Condition 3: N001- Acute nephritic syndrome with focal and segmental glomerular lesions Health Condition 4: N042- Nephrotic syndrome with diffuse membranous glomerulonephritis Health Condition 5: N045- Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis Health Conditi

Interventions

Intervention1: Losartan plus Enalapril: Primary glomerular disease patient who have received Tablet Losartan 100mg per day for atleast 4 weeks will be given Tablet Enalapril which will be uptitrated t

Sponsors

Department of Nephrology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with primary glomerular diseases â?? MN, FSGS, IgAn, iMPGN, MCD 2. Patients with who have received single RAAS blocking agent (LOSARTAN 100 mg) for atleast 4 weeks and having proteinuria more than 500 mg/day 3. Age >12 years 4. Either sex

Exclusion criteria

Exclusion criteria: 1. Secondary glomerulonephritis. 2. Prior history of angioedema 3. Bilateral renal artery stenosis 4. Pregnancy 5. Serum Potassium more than 5.1 mmol/L 6. eGFR < 30 ml/min

Design outcomes

Primary

MeasureTime frame
To evaluate the incidence and severity of adverse event related to RAAS inhibition in patients with primary glomerular diseasesTimepoint: 1 year

Secondary

MeasureTime frame
1. To study the decrease in proteinuria at the end of 1styear post randomization 2. To study the reduction in decline in eGFR at the end of 1styear post randomization 3. To study the incidence of other adverse events related to ACEI (dry cough, angioedema)Timepoint: 1 year

Countries

India

Contacts

Public ContactDr Tukaram Jamale

Seth GSMC and KEM hospital Mumbai

tukaramjamale@yahoo.co.in09167460362

Outcome results

None listed

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