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Effect of Hydroxychloroquine on Proteinuria and Inflammatory Markers in Chronic Glomerulopathy (CGN): A Randomized Controlled Trial

Effect of Hydroxychloroquine on Proteinuria and Inflammatory Markers in Chronic Glomerulopathy (CGN): A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250319019
Enrollment
36
Registered
2025-03-19
Start date
2024-04-02
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Chronic glomerulopathy patients with a urine protein to creatinine ratio (UPCR) more than or equal to 0.5 g/g and an estimated glomerular filtration rate (eGFR) of more than 20 mL/min/1.73 m2 Chronic glomerulopathy, hydroxychloroquine, proteinuria, interleukin-6

Interventions

Dose of hydroxychloroquine 200 mg orally (1 tablet) twice daily for patients with eGFR of more than 60 mL/min/1.73 m2, 300 mg orally (1.5 tablets) once daily for patients with eGFR between 45 and 59 m
Experimental Drug,Placebo Comparator Drug
Hydroxychloroquine (HCQ),Placebo

Sponsors

Department of Medicine, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 20 years, 2. A diagnosis of CGN from any causes with or without biopsy-proven CGN, 3. Estimated glomerular filtration rate (eGFR) of more than 20 mL/min/1.73 m2 (calculated using the Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI] creatinine equation), 4. Protein excretion of at least 0.50 grams per day despite receiving a maximum tolerable dose of renin-angiotensin-aldosterone system (RAAS) inhibitor for at least 3 months, 5. Inform consent

Exclusion criteria

Exclusion criteria: 1. Use of systemic immunosuppressive therapy except for maintenance low dose steroid at the time of enrollment, 2. An indication for a new regimen of corticosteroids (crescentic IgAN or minimal change disease with IgA deposits), 3. Contraindications for HCQ therapy, 4. Severe and uncontrolled comorbid diseases, 5. Current or planned pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Protein excretion At baseline, 2 months, and months after intervention Urine protein to creatinine ratio

Secondary

MeasureTime frame
Interleukin-6 At baseline, 2 months, and months after intervention Serum interleukin-6,High sensitivity C-reactive protein (hsCRP) At baseline, 2 months, and months after intervention Serum hsCRP,Glomerular filtration rate (GFR) At baseline, 2 months, and months after intervention Glomerular filtration rate (GFR)

Countries

Thailand

Contacts

Public ContactThitirat Supasil

Phramongkutklao hospital

thitirat_meaw@hotmail.com0817071114

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026