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Statins Evaluation in Coronary Procedures and Revascularization Trial (SECURE-PCI)

Primary Purpose

Acute Coronary Syndrome

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Atorvastatin
Placebo
Sponsored by
Hospital do Coracao
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute coronary syndrome patients intending to undergo percutaneous coronary intervention.

Exclusion Criteria:

  • Younger than 18 years
  • Presence of any contraindication to statin (Pregnant women, breast-feeding women or statin hypersensibility)
  • Advanced hepatic disease
  • Use of statins at the maximum dosage in the last 24 hours before the loading dose of the study drug
  • Use of fibrate in the last 24 hours

Sites / Locations

  • Hospital do Coracao

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Atorvastatin

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Major Cardiovascular Events (MACE)
All-cause mortality, nonfatal acute myocardial infarction, stroke or revascularization with either percutaneous coronary intervention or coronary artery bypass grafting

Secondary Outcome Measures

Major Cardiovascular Events (MACE)
All-cause mortality
Non-fatal Myocardial Infarction
Non-fatal Stroke
Revascularization
Cardiovascular death
Stent Thrombosis
Target vessel revascularization
Rhabdomyolysis
Bleeding episode

Full Information

First Posted
October 6, 2011
Last Updated
June 14, 2019
Sponsor
Hospital do Coracao
Collaborators
Ministry of Health, Brazil
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1. Study Identification

Unique Protocol Identification Number
NCT01448642
Brief Title
Statins Evaluation in Coronary Procedures and Revascularization Trial
Acronym
SECURE-PCI
Official Title
A Randomized, Multicenter Clinical Trial to Assess the Effect of Atorvastatin in Patients With Acute Coronary Syndrome and Intended Percutaneous Coronary Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
April 2012 (Actual)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital do Coracao
Collaborators
Ministry of Health, Brazil

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether a loading dose of atorvastatin before percutaneous intervention procedures in acute coronary syndromes is effective to reduce major cardiovascular events(MACE).
Detailed Description
Background: Strategies to reduce complications in acute coronary syndrome treatment have been largely studied. Due to its pleiotropic effects statins are considered an important tool on atherosclerotic plaque stability. Although, the usage of statins before percutaneous coronary intervention in acute coronary syndrome patients, has not yet been demonstrated. Objectives: Evaluate if a loading dose of atorvastatin (80mg) before percutaneous coronary intervention in acute coronary syndrome patients, followed by a reload dose 24 hours, is able to reduce major cardiovascular events (MACE); including combined outcomes such as all-cause mortality, nonfatal acute myocardial infarction, stroke or revascularization with either percutaneous coronary intervention or coronary-artery bypass grafting after 30 days. Methods: Multicentric randomised controlled clinical trial, with allocation concealment and intention to treat analysis. Competitive recruitment will involve 4,192 patients. Acute coronary syndrome patients intending to undergo percutaneous coronary intervention with or without stent placement will be randomized 1:1 to receive either atorvastatin 80mg or placebo before the coronary procedure and also a reload dosage after 24 hours from angioplasty. All patients will collect blood sample to determine CKMB levels pre and post procedure (6 to 12h and 18 to 24 hours). After 30 days, an in person interview will be performed and blood sample will be collected in order to dosage AST, ALT, CPK, and cholesterol levels. Telephonic interview will be done at 6 and 12 months to access occurrence of cardiovascular events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
4191 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Intervention Description
Atorvastatin loading dose of 80mg before PCI, reloading dose of 80mg 24 hours after PCI, and atorvastatin 40mg for 30 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matching placebo before PCI and 24 hours after PCI. Atorvastatin 40mg for 30 days
Primary Outcome Measure Information:
Title
Major Cardiovascular Events (MACE)
Description
All-cause mortality, nonfatal acute myocardial infarction, stroke or revascularization with either percutaneous coronary intervention or coronary artery bypass grafting
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Major Cardiovascular Events (MACE)
Time Frame
6 months and 12 months
Title
All-cause mortality
Time Frame
30 days, 6 months and 12 months
Title
Non-fatal Myocardial Infarction
Time Frame
30 days, 6 months and 12 months
Title
Non-fatal Stroke
Time Frame
30 days, 6 months and 12 months
Title
Revascularization
Time Frame
30 days, 6 months and 12 months
Title
Cardiovascular death
Time Frame
30 days, 6 months and 12 months
Title
Stent Thrombosis
Time Frame
30 days, 6 months and 12 months
Title
Target vessel revascularization
Time Frame
30 days, 6 months and 12 months
Title
Rhabdomyolysis
Time Frame
7 days or at hospital discharge
Title
Bleeding episode
Time Frame
7 days or hospital discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute coronary syndrome patients intending to undergo percutaneous coronary intervention. Exclusion Criteria: Younger than 18 years Presence of any contraindication to statin (Pregnant women, breast-feeding women or statin hypersensibility) Advanced hepatic disease Use of statins at the maximum dosage in the last 24 hours before the loading dose of the study drug Use of fibrate in the last 24 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Otavio Berwanger
Organizational Affiliation
Hospital do Coracao
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Renato D Lopes, MD, PhD
Organizational Affiliation
Brazilian Clinical Research Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital do Coracao
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
04005-000
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
29525821
Citation
Berwanger O, Santucci EV, de Barros E Silva PGM, Jesuino IA, Damiani LP, Barbosa LM, Santos RHN, Laranjeira LN, Egydio FM, Borges de Oliveira JA, Dall Orto FTC, Beraldo de Andrade P, Bienert IRC, Bosso CE, Mangione JA, Polanczyk CA, Sousa AGMR, Kalil RAK, Santos LM, Sposito AC, Rech RL, Sousa ACS, Baldissera F, Nascimento BR, Giraldez RRCV, Cavalcanti AB, Pereira SB, Mattos LA, Armaganijan LV, Guimaraes HP, Sousa JEMR, Alexander JH, Granger CB, Lopes RD; SECURE-PCI Investigators. Effect of Loading Dose of Atorvastatin Prior to Planned Percutaneous Coronary Intervention on Major Adverse Cardiovascular Events in Acute Coronary Syndrome: The SECURE-PCI Randomized Clinical Trial. JAMA. 2018 Apr 3;319(13):1331-1340. doi: 10.1001/jama.2018.2444. Erratum In: JAMA. 2018 Sep 4;320(9):938.
Results Reference
result
PubMed Identifier
30264159
Citation
Lopes RD, de Barros E Silva PGM, de Andrade Jesuino I, Santucci EV, Barbosa LM, Damiani LP, Nakagawa Santos RH, Laranjeira LN, Dall Orto FTC, Beraldo de Andrade P, de Castro Bienert IR, Alexander JH, Granger CB, Berwanger O. Timing of Loading Dose of Atorvastatin in Patients Undergoing Percutaneous Coronary Intervention for Acute Coronary Syndromes: Insights From the SECURE-PCI Randomized Clinical Trial. JAMA Cardiol. 2018 Nov 1;3(11):1113-1118. doi: 10.1001/jamacardio.2018.3408. Erratum In: JAMA Cardiol. 2018 Nov 1;3(11):1131.
Results Reference
derived
PubMed Identifier
29653634
Citation
Berwanger O, de Barros E Silva PGM, Dall Orto FTC, de Andrade PB, de Castro Bienert IR, Bosso CE, Mangione J, Polanczyk CA, Sousa A, Kalil R, de Moura Santos L, Sposito AC, Rech RL, Sousa ACS, Baldissera F, Nascimento BR, de Andrade Jesuino I, Santucci EV, Damiani LP, Laranjeira LN, Borges de Oliveira JA, Giraldez RR, Cavalcanti AB, Pereira SB, Mattos LA, Armaganijan LV, Guimaraes HP, Sousa JE, Alexander JH, Granger CB, Lopes RD. Rationale and design of the Statins Evaluation in Coronary procedUres and REvascularization: The SECURE-PCI Trial. Am Heart J. 2018 Apr;198:129-134. doi: 10.1016/j.ahj.2017.12.018. Epub 2018 Jan 8.
Results Reference
derived

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Statins Evaluation in Coronary Procedures and Revascularization Trial

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