search
Back to results

Standard Clopidogrel Versus Prasugrel Low Dose Therapy in Elderly Patients With Acute Coronary Syndrome (RESET ELDERLY)

Primary Purpose

Coronary Artery Disease

Status
Unknown status
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Clopidogrel
Prasugrel
Sponsored by
Gennaro Sardella
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring antiplatelet effect, prasugrel, clopidogrel, acute coronary syndrome

Eligibility Criteria

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

Inclusion Criteria:

  • Acute coronary syndrome
  • PCI with stent implantation
  • clopidogrel responsiveness
  • > 75 years of age.

Exclusion Criteria:

  • history of bleeding diathesis
  • chronic oral anticoagulation treatment
  • contraindications to antiplatelet therapy
  • PCI or coronary artery bypass grafting (CABG) < 3 months
  • hemodynamic instability
  • platelet count < 100,000/μl
  • hematocrit < 30%
  • creatinine clearance < 25 ml/min
  • Patients with a history of stroke
  • other contraindication for prasugrel administration
  • patients weighing < 60 kg
  • high on treatment platelet reactivity

Sites / Locations

  • Dept.of Cardiovascular Sciences,Policlinico Umberto I

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Prasugrel low dose

Clopidogrel standard dose

Arm Description

Patient will be randomized to this intervention will receive prasugrel 5 mg and after 15 days and 30 days we will control the responsivness of the study drug.

Patient will be randomized to this intervention will receive clopidogrel 75 mg and after 15 days and 30 days we will control the responsivness of the study drug.

Outcomes

Primary Outcome Measures

superiority of prasugrel low dose
The primary aim will be to investigate the antiplatelet effect of half dose of prasugrel (5 mg) versus standard dose of clopidogrel in patients with acute coronary syndrome and coronary diseases, treated with percutaneous coronary intervention and stent implantation.

Secondary Outcome Measures

Bleeding
Bleeding (major, minor, or minimal according to the TIMI study criteria)
major adverse cardiac events
major adverse cardiac events (cardiovascular death, myocardial infarction, and stroke) will be evaluated during the all period of treatment.

Full Information

First Posted
January 24, 2013
Last Updated
January 24, 2013
Sponsor
Gennaro Sardella
search

1. Study Identification

Unique Protocol Identification Number
NCT01778842
Brief Title
Standard Clopidogrel Versus Prasugrel Low Dose Therapy in Elderly Patients With Acute Coronary Syndrome
Acronym
RESET ELDERLY
Official Title
PhaRmacodynamic Effect of Antiplatelet Agents in Elderly Patients: Standard Clopidogrel Versus prasugrEl Low Dose Therapy.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Unknown status
Study Start Date
March 2013 (undefined)
Primary Completion Date
June 2013 (Anticipated)
Study Completion Date
July 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Gennaro Sardella

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The elderly represent a growing segment of the coronary population treated by dual antiplatelet therapy for percutaneous coronary intervention (PCI). These patients bear a higher risk of both ischemic events and bleeding complications than younger patients, with a subsequently higher rate of mortality.Recentprogress in antithrombotic treatment demonstrated the efficacy of adding a P2Y12 receptor antagonist to low-dose aspirin. Whether this benefit is also present in the elderly remains a debated issue due to the lack of specific data in this sub-population. The present study was realized to provide specific data on platelet response to clopidogrel, standard dose (75 mg) or prasugrel 5 mg in elderly patients (≥75 years old) whereas the superiority in PR response of the latter should allows the Prasugrel therapy in elderly patients with the better clinical efficacy and therapeutical safety already showed compared with Clopidogrel.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
antiplatelet effect, prasugrel, clopidogrel, acute coronary syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
68 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prasugrel low dose
Arm Type
Experimental
Arm Description
Patient will be randomized to this intervention will receive prasugrel 5 mg and after 15 days and 30 days we will control the responsivness of the study drug.
Arm Title
Clopidogrel standard dose
Arm Type
Experimental
Arm Description
Patient will be randomized to this intervention will receive clopidogrel 75 mg and after 15 days and 30 days we will control the responsivness of the study drug.
Intervention Type
Drug
Intervention Name(s)
Clopidogrel
Intervention Description
Patient will be randomized to this intervention will receive the standard dose of clopidogrel and after 15 days and 30 days we will control the responsivness of the study drug.
Intervention Type
Drug
Intervention Name(s)
Prasugrel
Intervention Description
Patient will be randomized to this intervention will receive the low dose of prasugrel and after 15 days and 30 days we will control the responsivness of the study drug.
Primary Outcome Measure Information:
Title
superiority of prasugrel low dose
Description
The primary aim will be to investigate the antiplatelet effect of half dose of prasugrel (5 mg) versus standard dose of clopidogrel in patients with acute coronary syndrome and coronary diseases, treated with percutaneous coronary intervention and stent implantation.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Bleeding
Description
Bleeding (major, minor, or minimal according to the TIMI study criteria)
Time Frame
12 months
Title
major adverse cardiac events
Description
major adverse cardiac events (cardiovascular death, myocardial infarction, and stroke) will be evaluated during the all period of treatment.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute coronary syndrome PCI with stent implantation clopidogrel responsiveness > 75 years of age. Exclusion Criteria: history of bleeding diathesis chronic oral anticoagulation treatment contraindications to antiplatelet therapy PCI or coronary artery bypass grafting (CABG) < 3 months hemodynamic instability platelet count < 100,000/μl hematocrit < 30% creatinine clearance < 25 ml/min Patients with a history of stroke other contraindication for prasugrel administration patients weighing < 60 kg high on treatment platelet reactivity
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gennaro Sardella, MD
Phone
+390649979035
Email
rino.sardella@uniroma1.it
Facility Information:
Facility Name
Dept.of Cardiovascular Sciences,Policlinico Umberto I
City
Rome
ZIP/Postal Code
000161
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rocco Stio, MD
Phone
+300649979046
Email
rocco.stio@libero.it

12. IPD Sharing Statement

Learn more about this trial

Standard Clopidogrel Versus Prasugrel Low Dose Therapy in Elderly Patients With Acute Coronary Syndrome

We'll reach out to this number within 24 hrs