Statin Contrast Induced Nephropathy Prevention (PRATO-ACS)
Primary Purpose
Acute Coronary Syndrome
Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Rosuvastatin
Sponsored by
About this trial
This is an interventional prevention trial for Acute Coronary Syndrome focused on measuring statin, CIN, periprocedural damage
Eligibility Criteria
Inclusion Criteria:
Are eligible for the study all patients admitted to CCU for Acute Coronary Syndrome without ST elevation (NSTEMI) candidates for early invasive strategy (coronary angiography within 48 hours from the admission) and without previous therapy with statins.
Exclusion Criteria:
- inability to provide consent
- pregnancy or lactation
- intolerance to statins
- therapy with other lipid lowering drugs
- acute or chronic liver disease
- chronic muscle disease
- acute renal failure or chronic renal failure stage IV
- neoplastic
- exposure to iodinated contrast medium in the previous 10 days
Sites / Locations
- Cardiology Division, Prato Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Rosuvastatin
Control
Arm Description
Outcomes
Primary Outcome Measures
Incidence of contrast-induced nephropathy in patients with Acute Coronary Syndrome treated with rosuvastatin versus control
Secondary Outcome Measures
Peak levels and curve areas of myocardial necrosis markers measured throughout the hospitalization period.
Quantitative creatine kinase-MB (CK-MB) mass and cTn I were measured at admission and at 6, 12, and 24 hours during the first day then once daily, immediately before angiography, and 24 hours thereafter. In patients who underwent angioplasty, biochemical markers were measured at 12 and 24 hours after procedure.
Distribution of peripheral lymphocyte populations at the entry and at discharge
Comparison between groups for the distribution of peripheral lymphocyte sub-population evaluated bu Flow Cytometric Analysis at the admission and at discharge.
Incidence of clinical composite outcome (death, myocardial infarction, urgent revascularization, dialysis and stroke).
Clinical follow-up at 30 days and 6 month after the hospitalization for the Acute Coronary Syndrome.
Full Information
NCT ID
NCT01185938
First Posted
August 3, 2010
Last Updated
October 18, 2012
Sponsor
Centro Cardiopatici Toscani
1. Study Identification
Unique Protocol Identification Number
NCT01185938
Brief Title
Statin Contrast Induced Nephropathy Prevention
Acronym
PRATO-ACS
Official Title
Protective Effect of Rosuvastatin and Antiplatelet Therapy On Contrast-induced Nephropathy and Myocardial Damage in Patients With Acute Coronary Syndrome Undergoing Coronary Intervention; PRATO-ACS Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
October 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Cardiopatici Toscani
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This open-label study, prospective, randomized trial evaluating the acute (in-hospital) pleiotropic and clinical effects of a hydrophilic statin (rosuvastatin) in patients with acute coronary syndrome
Detailed Description
The primary purpose of this study is to determine whether, in patients with acute coronary syndromes not taking statins in chronic administration, high doses of a hydrophilic statin (rosuvastatin) administered before coronary angiography and/or angioplasty, may exert a renal-protective effect by reducing the incidence of contrast nephropathy. Contrast induced nephropathy is defined as increased values of creatinine >= 0.3 mg/dl from baseline values, within 72 hours after contrast medium exposure.
Secondary end points: 1) verify if short-term (<48 hours)statin administration reduces the peak levels and the curve areas of markers of myocardial necrosis throughout the hospitalization period and if reduces the occurrence of periprocedural infarction. Biochemical markers (quantitative creatine kinase-MB (CK-MB) mass and Troponin I) are measured at admission and at 6, 12, and 24 hours during the first day then once daily, immediately before angiography, and 24 hours thereafter. In patients who underwent coronary angioplasty (PCI), biochemical markers were measured at 12 and 24 hours after the procedure. Data were fitted, peak values and curve areas calculated; the occurrence of periprocedural infarction was defined as a CK-MB mass elevation more than three times the upper limit of normal within 24 hours after PCI. 2) determine the distribution of peripheral lymphocytic populations at the entry and at discharge using the flow cytometric analysis; 3) analyze the clinical composite outcome of death, myocardial infarction, urgent revascularization, dialysis and stroke at 30 days and 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome
Keywords
statin, CIN, periprocedural damage
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rosuvastatin
Arm Type
Active Comparator
Arm Title
Control
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Description
One oral single dose of rosuvastatin of 40 mg at admission and then 20 mg/day for 1 month.
Primary Outcome Measure Information:
Title
Incidence of contrast-induced nephropathy in patients with Acute Coronary Syndrome treated with rosuvastatin versus control
Time Frame
3 days
Secondary Outcome Measure Information:
Title
Peak levels and curve areas of myocardial necrosis markers measured throughout the hospitalization period.
Description
Quantitative creatine kinase-MB (CK-MB) mass and cTn I were measured at admission and at 6, 12, and 24 hours during the first day then once daily, immediately before angiography, and 24 hours thereafter. In patients who underwent angioplasty, biochemical markers were measured at 12 and 24 hours after procedure.
Time Frame
5 days (average)
Title
Distribution of peripheral lymphocyte populations at the entry and at discharge
Description
Comparison between groups for the distribution of peripheral lymphocyte sub-population evaluated bu Flow Cytometric Analysis at the admission and at discharge.
Time Frame
5 days (average)
Title
Incidence of clinical composite outcome (death, myocardial infarction, urgent revascularization, dialysis and stroke).
Description
Clinical follow-up at 30 days and 6 month after the hospitalization for the Acute Coronary Syndrome.
Time Frame
30 days and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Are eligible for the study all patients admitted to CCU for Acute Coronary Syndrome without ST elevation (NSTEMI) candidates for early invasive strategy (coronary angiography within 48 hours from the admission) and without previous therapy with statins.
Exclusion Criteria:
inability to provide consent
pregnancy or lactation
intolerance to statins
therapy with other lipid lowering drugs
acute or chronic liver disease
chronic muscle disease
acute renal failure or chronic renal failure stage IV
neoplastic
exposure to iodinated contrast medium in the previous 10 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna Toso, MD
Organizational Affiliation
Misericordia e Dolce, Prato Hospital, Cardiology Unit
Official's Role
Study Chair
Facility Information:
Facility Name
Cardiology Division, Prato Hospital
City
Prato
ZIP/Postal Code
59100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
25523533
Citation
Toso A, Leoncini M, Maioli M, Tropeano F, Di Vincenzo E, Villani S, Bellandi F. Relationship between inflammation and benefits of early high-dose rosuvastatin on contrast-induced nephropathy in patients with acute coronary syndrome: the pathophysiological link in the PRATO-ACS study (Protective Effect of Rosuvastatin and Antiplatelet Therapy on Contrast-Induced Nephropathy and Myocardial Damage in Patients With Acute Coronary Syndrome Undergoing Coronary Intervention). JACC Cardiovasc Interv. 2014 Dec;7(12):1421-9. doi: 10.1016/j.jcin.2014.06.023.
Results Reference
derived
PubMed Identifier
25440809
Citation
Leoncini M, Toso A, Maioli M, Tropeano F, Badia T, Villani S, Bellandi F. Early high-dose rosuvastatin and cardioprotection in the protective effect of rosuvastatin and antiplatelet therapy on contrast-induced acute kidney injury and myocardial damage in patients with acute coronary syndrome (PRATO-ACS) study. Am Heart J. 2014 Nov;168(5):792-7. doi: 10.1016/j.ahj.2014.08.005. Epub 2014 Aug 10.
Results Reference
derived
PubMed Identifier
24076283
Citation
Leoncini M, Toso A, Maioli M, Tropeano F, Villani S, Bellandi F. Early high-dose rosuvastatin for contrast-induced nephropathy prevention in acute coronary syndrome: Results from the PRATO-ACS Study (Protective Effect of Rosuvastatin and Antiplatelet Therapy On contrast-induced acute kidney injury and myocardial damage in patients with Acute Coronary Syndrome). J Am Coll Cardiol. 2014 Jan 7-14;63(1):71-9. doi: 10.1016/j.jacc.2013.04.105. Epub 2013 Sep 26.
Results Reference
derived
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Statin Contrast Induced Nephropathy Prevention
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