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To evaluate the efficacy of the ACE inhibitor ramipril in the treatment of early IgA nephropathy.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Ramipril |
|
| 2 | No Intervention |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ramipril | Drug | 2.5mg and increase to 5mg if patient do not develop symptomatic hypotension |
|
| Measure | Description | Time Frame |
|---|---|---|
| Development of hypertension (defined as blood pressure above 140/90 mm Hg and require anti-hypertensive therapy) | From the beginning to the end of the study | |
| Development of proteinuria | From the beginning to the end of the study | |
| 20% decline in creatinine clearance, as determined by 24-hour urine collection or estimated by the Gault-Cockroft equation | From the beginning to the end of the study | |
| body weight, blood pressure, pulse | From the beginning to the end of the study | |
| Adverse effects of treatment | From the beginning to the end of the study |
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Inclusion Criteria:
Exclusion Criteria:
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
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| Name | Affiliation | Role |
|---|---|---|
| Daniel Yuen | Sanofi | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sanofi-Aventis | Hong Kong | Hong Kong |
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| ID | Term |
|---|---|
| D005921 | Glomerulonephritis |
| ID | Term |
|---|---|
| D009393 | Nephritis |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| ID | Term |
|---|---|
| D017257 | Ramipril |
| ID | Term |
|---|---|
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |