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Atorvastatin and Clopidogrel HIgh DOse in Stable Patients With Residual High Platelet Activity (ACHIDO)

Primary Purpose

Stable Angina

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
atorvastatin and clopidogrel
Clopidogrel
Sponsored by
Ospedale Misericordia e Dolce
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stable Angina focused on measuring Clopidogrel, Statins, Platelet reactivity, Point-of-care platelet function test

Eligibility Criteria

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

Inclusion Criteria:

  • Stable angina
  • candidates to drug eluting stent implantation
  • High on-treatment platelet reactivity according to a point-of-care platelet function test

Exclusion Criteria:

  • chronic therapy with statins
  • inability to provide informed consent
  • intolerance to statins
  • acute or chronic liver failure or ALT > 2 times ULN
  • known myopathy
  • CKD stage IV or dialysis treatment
  • pregnancy or breast-feeding
  • malignancy

Sites / Locations

  • Cardiology Department, Ospedale Misericordia e Dolce

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Atorvastatin-Clopidogrel group

Clopidogrel group

Arm Description

Patients who receive Atorvastatin 80 mg/day and Clopidogrel 150 mg/day

Patients who receive clopidogrel 150 mg daily

Outcomes

Primary Outcome Measures

Change from baseline in on-treatment platelet reactivity at 7 and 30 days
Pharmacodynamic analysis of the randomized groups includes a) assessment of the absolute level of on-treatment reactivity, b) change in on-treatment reactivity, c) rate of high on-treatment reactivity at 7 and 30 days. The platelet reactivity is measured with the VerifyNow P2Y12 test (Accumetrics, SanDiego, CA).

Secondary Outcome Measures

Full Information

First Posted
April 11, 2011
Last Updated
January 24, 2012
Sponsor
Ospedale Misericordia e Dolce
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1. Study Identification

Unique Protocol Identification Number
NCT01335048
Brief Title
Atorvastatin and Clopidogrel HIgh DOse in Stable Patients With Residual High Platelet Activity
Acronym
ACHIDO
Official Title
Atorvastatin and Clopidogrel HIgh DOse in Stable Patients With Residual High Platelet Activity
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ospedale Misericordia e Dolce

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate if high-dose (80mg/day) atorvastatin might exert an adjunctive anti-platelet effect compared to high-dose clopidogrel (150mg/day) in stable patients with high on-treatment reactivity according to a point-of-care platelet function assay.
Detailed Description
This is a prospective, randomized, open-label, control-active trial performed in elective patients candidates to coronary drug eluting stent implantation who presented high-on-treatment platelet reactivity, immediately before coronary intervention (PCI). All patients are treated with aspirin (100 mg/day) and standard-dose clopidogrel (600 mg as loading dose and 75 mg daily as maintenance dose)for at least 7 days before PCI. Platelet function is assessed by the VerifyNow P2Y12 assay (Accumetrics, San Diego, CA). Patients are eligible to be enrolled if they have high-on-treatment reactivity defined as P2Y12 reaction units (PRU) >= 230, immediately before PCI. After PCI, patients are randomized to receive high-dose clopidogrel (150 mg daily) or high-dose atorvastatin (80mg/day) + high-dose clopidogrel (150 mg daily). Study visits and platelet function testing with the VerifyNow P2Y12 test are conducted at 7 and 30 days after randomization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stable Angina
Keywords
Clopidogrel, Statins, Platelet reactivity, Point-of-care platelet function test

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin-Clopidogrel group
Arm Type
Experimental
Arm Description
Patients who receive Atorvastatin 80 mg/day and Clopidogrel 150 mg/day
Arm Title
Clopidogrel group
Arm Type
Active Comparator
Arm Description
Patients who receive clopidogrel 150 mg daily
Intervention Type
Drug
Intervention Name(s)
atorvastatin and clopidogrel
Intervention Description
Atorvastatin 80 mg daily + clopidogrel 150 mg daily
Intervention Type
Drug
Intervention Name(s)
Clopidogrel
Intervention Description
Clopidogrel 150 mg daily
Primary Outcome Measure Information:
Title
Change from baseline in on-treatment platelet reactivity at 7 and 30 days
Description
Pharmacodynamic analysis of the randomized groups includes a) assessment of the absolute level of on-treatment reactivity, b) change in on-treatment reactivity, c) rate of high on-treatment reactivity at 7 and 30 days. The platelet reactivity is measured with the VerifyNow P2Y12 test (Accumetrics, SanDiego, CA).
Time Frame
pre-PCI, 7 days and 30 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stable angina candidates to drug eluting stent implantation High on-treatment platelet reactivity according to a point-of-care platelet function test Exclusion Criteria: chronic therapy with statins inability to provide informed consent intolerance to statins acute or chronic liver failure or ALT > 2 times ULN known myopathy CKD stage IV or dialysis treatment pregnancy or breast-feeding malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario Leoncini, MD
Organizational Affiliation
Ospedale Misericordia e Dolce, Prato
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anna Toso, MD
Organizational Affiliation
Ospedale Misericordia e Dolce, Prato
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cardiology Department, Ospedale Misericordia e Dolce
City
Prato
ZIP/Postal Code
59100
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
23428009
Citation
Leoncini M, Toso A, Maioli M, Angiolillo DJ, Giusti B, Marcucci R, Abbate R, Bellandi F. High-dose atorvastatin on the pharmacodynamic effects of double-dose clopidogrel in patients undergoing percutaneous coronary interventions: The ACHIDO (Atorvastatin and Clopidogrel HIgh DOse in stable patients with residual high platelet activity) study. JACC Cardiovasc Interv. 2013 Feb;6(2):169-79. doi: 10.1016/j.jcin.2012.09.013.
Results Reference
derived

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Atorvastatin and Clopidogrel HIgh DOse in Stable Patients With Residual High Platelet Activity

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