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Pharmacological intervention of Atorvastatin vs. Rosvastatin in patients with Acute coronary Syndrome (ATRAS study)

Pharmacological intervention of Atorvastatin vs. Rosvastatin in patients with Acute coronary Syndrome (ATRAS study) - ATRAS study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004200
Enrollment
100
Registered
2010-09-13
Start date
2008-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Coronary Artery Disease

Interventions

Atorvastatin (10mg/day). Study preriod is Dec. 2008-Sep. 2010. Rosvastatin (2.5mg/day) Study preriod is Dec. 2008-Sep. 2010.

Sponsors

Division of cardiology, Department of Internal Medicine, Memorial Heart Center, Iwate Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1) Coroanry artery disease with hyperlipidemia, 2) Acceptable for prescription of Atorvastatin and rosvastatin 3) ACC/AHA guideline diagnositic criteria (J Am Coll Cardiol. 2002;40:1366-74) 4) Patients after coronary intervention 5) Acceptable follow up in our center 6) Age: over 20 years old 7) Sex: undetermined

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1) stand by scheduled CABG during study period 2) valvelar heart disease 3) chronic lung disease, cor plumonale 4) poor prognosis disease (malignant tumor etc.) within 5 years 5) bilateral renal artery stenosis, one-side kidney and renal artery stenosis, high potassium (K 5.0mEq/L), renal insufficiency (creatine 3.0mg/dL), liver dysfunction (AST>100 U/L, ALT>100U/L), anemia (Hb <6.0mg/dL) 6) in pregnancy (including suspicious state) , the lactation period 7) drug allergy for HMG-CoA reductase inhibitor 8) contraindication of HMG-CoA reductase inhibitor 9) could not obtained written informed consent 10) unfavorable patient for this study protocol

Design outcomes

Primary

MeasureTime frame
1:plaque evaluation using IVUS 2:EPC function, immunological response of monocyto 3:all cause death, all cause cardiovascular event 4:repeat revascularization

Countries

Japan

Contacts

Public ContactTomonori Itoh

Iwate Medical University Division of cardiology, Department of Internal Medicine, Memorial Heart Center

tomoitoh@iwate-med.ac.jp019-651-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026