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Study of Atorvastatin Dose Dependent Reduction of Proteinuria

The Renal Protective Effects of Low-dose and High-dose Atorvastatin in Patients With Glomerular Disease and Proteinuria: a Randomized Controlled Double Blinded Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00768638
Acronym
SARP
Enrollment
23
Registered
2008-10-08
Start date
2008-10-31
Completion date
2014-06-30
Last updated
2015-04-29

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

Conditions

Chronic Kidney Disease

Keywords

Chronic kidney disease

Brief summary

Randomized controlled double blind study of parallel groups to evaluate the comparative effects of low-dose of atorvastatin on proteinuria in patients with stage 3 or 4 chronic kidney disease.

Interventions

DRUGAtorvastatin

Atorvastatin 10mg 1co id (10mg active) Placebo 40mg 1co id (40mg inactive)

Sponsors

Laval University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age of 18 and over * Stage 3 or 4 chronic kidney disease (modified MDRD) * proteinuria of \> 1g/d on ACEi and/or ARB, or proteinuria of \> 1g/d with intolerance or contraindication to ACEi and/or ARB * blood pressure \< 130/80 mmHg or \< 140/90 mmHg in patients with five or more antihypertensive drugs * stable renal function

Exclusion criteria

* rapid progression of renal failure * immunosuppressive therapy within the past 3 months * need a renal replacement therapy within 8 months * definite history of chronic liver disease, or abnormal liver function * evidence of active inflammatory muscle disease * definite previous adverse reaction to a statin * concurrent treatment with a contraindicated drug (fibrate, macrolide antibiotic, systemic use of imidazole or triazole antifungals, protease-inhibitors, ciclosporin) * child bearing potential * known to be poorly compliant with clinic visits or prescribed medication

Design outcomes

Primary

MeasureTime frame
proteinuria6 months

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026