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Completed Phase 2 Interventional Results available

Prospective Evaluation of Proteinuria and Renal Function in Diabetic Patients With Progressive Renal Disease

ClinicalTrials.gov ID: NCT00296374

Public ClinicalTrials.gov record NCT00296374. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomised, Double-blind, 52-wk, Parallel-grp, Multicentre, PIIb Study to Evaluate Effects of Rosuvastatin 10mg, Rosuvastatin 40mg and Atorvastatin 80mg on Urinary Protein Excretion in Hypercholesterolaemic Diabetic Patients With Moderate Proteinuria

Study identification

NCT ID
NCT00296374
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
353 participants

Conditions and interventions

Interventions

  • Rosuvastatin Drug
  • Atorvastatin Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2006
Primary completion
Feb 28, 2009
Completion
Feb 28, 2009
Last update posted
Aug 31, 2011

2006 – 2009

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Research Site Avondale Arizona
Research Site Phoenix Arizona
Research Site Jonesboro Arkansas
Research Site Pasadena California
Research Site Riverside California
Research Site Santa Ana California
Research Site West Hills California
Research Site Hollywood Florida
Research Site Jacksonville Florida
Research Site West Palm Beach Florida
Research Site Augusta Georgia
Research Site Topeka Kansas
Research Site Springfield Massachusetts
Research Site Detroit Michigan
Research Site Columbia Missouri
Research Site St Louis Missouri
Research Site Orchard Park New York
Research Site Stony Brook New York
Research Site Winston-Salem North Carolina
Research Site Cincinnati Ohio
Research Site Kettering Ohio
Research Site Pittsburgh Pennsylvania
Research Site Columbia South Carolina
Research Site Dallas Texas
Research Site Houston Texas
Research Site Lubbock Texas
Research Site San Antonio Texas
Research Site Ogden Utah
Research Site Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 87 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00296374, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 31, 2011 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00296374 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →