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A multicentre randomised controlled study of the efficacy and safety of cotrimoxazole in the prophylaxis of moricinol ester in the treatment of glomerulonephritis infections

A multicentre randomised controlled study of the efficacy and safety of cotrimoxazole in the prophylaxis of moricinol ester in the treatment of glomerulonephritis infections

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091406
Enrollment
Unknown
Registered
2024-10-28
Start date
2024-10-28
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

glomerular disease

Interventions

cotimoxazole group:Receive mycophenolate mofetil(MMF) at 1-2 g/d for =12 weeks. Oral cotrimoxazole was initiated on the same day as the MMF treatment and was administered orally as 1 tablet once daily
Non-cotrimoxazole group:Receivemycophenolate mofetil(MMF) at 1-2 g/d for =12 weeks. No prophylactic application of cotrimoxazole.

Sponsors

The First Affiliated Hospital of the Air Force Military Medical University of the People's Liberation Army of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Written informed consent was obtained; (2) Aged 18-80 years; (3) Patients with a confirmed diagnosis of glomerulonephritis (both primary and secondary glomerulonephritis) who are also receiving MMF treatment at the same time.

Exclusion criteria

Exclusion criteria: (1) Hypersensitivity to sulfamethoxazole and methotrexate components; (2) Evidence of active infection within 3 weeks before enrolment; (3) Use of antimicrobial drugs within 10 days before enrolment; (4) Combination of other diseases: positive serological index of HBV; congenital or acquired immunodeficiency; active infection or clinical evidence of active tuberculosis or active cytomegalovirus infection; history of peptic ulcer and/or gastrointestinal bleeding; agranulocytosis; malignant neoplasm; serious cardiovascular diseases such as congenital heart disease, arrhythmia, heart failure; serious mental illness; (5) Women of childbearing age who are pregnant, have failed to use contraception, are breastfeeding, or are unable or unwilling to use adequate contraception. (6) Administer steroids and cyclophosphamide for the first three months of enrollment.

Design outcomes

Primary

MeasureTime frame
Routine blood test;urine routine;urinate frequently;kidney function;haemonium;blood lipid;immunoglobulin;complement;blood sedimentation;C-reactive protein;Calcitoninogen; interleukin-6;blood endotoxin quantification (LPS);galactomannan test;

Secondary

MeasureTime frame
Blood 1,3-ß-D glucan;

Countries

china

Contacts

Public Contactlijie He

Xijing Hospital

43218204@qq.com+86 150 9118 5737

Outcome results

None listed

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