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Time Based Strategy to Reduce Clopidogrel Associated Bleeding Related to Coronary Artery Bypass Graft (CABG) (TARGET-CABG)

Primary Purpose

Coronary Artery Disease

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Clopidogrel withdraw prior to CABG
Sponsored by
LifeBridge Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Coronary Artery Disease focused on measuring Coronary Artery Disease, CABG, Clopidogrel, Aspirin, Point of Care devices

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must provide written informed consent.
  • Patients must currently be on aspirin therapy (81-325 mg).
  • Male or female patients between the ages of 18-85 requiring CABG.

Exclusion Criteria:

  • Patients undergoing emergent surgery following failed percutaneous coronary revascularization.
  • Patients with a history of previous cardiac surgery and patients needing concomitant valvular surgery.
  • Pre-operative exposure to either coumadin or platelet GPIIb/IIIa inhibitors.
  • Patients with a history of bleeding diathesis.
  • Patients with an activated partial thrombin time >1.5 normal.
  • Patients with platelet count <120,000/mm3.
  • Patients with hematocrit <30%.
  • Patients with creatinine clearance <30mL/min.
  • Patients with known active hepatic disease.
  • Patients with any other condition that, in the opinion of the investigator, may either put the patient at risk or influence the result of the study (e.g. malignancy, limiting life expectancy, noncompliance).

Sites / Locations

  • Sinai HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Aspirin only

Clopidogrel and Aspirin

Arm Description

Continue aspirin until surgery

Outcomes

Primary Outcome Measures

The primary endpoint is chest tube drainage.

Secondary Outcome Measures

The secondary endpoint is transfusion requirements.

Full Information

First Posted
March 4, 2009
Last Updated
March 5, 2009
Sponsor
LifeBridge Health
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1. Study Identification

Unique Protocol Identification Number
NCT00857155
Brief Title
Time Based Strategy to Reduce Clopidogrel Associated Bleeding Related to Coronary Artery Bypass Graft (CABG)
Acronym
TARGET-CABG
Study Type
Interventional

2. Study Status

Record Verification Date
March 2009
Overall Recruitment Status
Unknown status
Study Start Date
January 2009 (undefined)
Primary Completion Date
January 2011 (Anticipated)
Study Completion Date
February 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
LifeBridge Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose: In patients with coronary artery disease, aspirin and Plavix are used increasingly to prevent the formation of blood clots in the coronary arteries. These drugs exert their beneficial effects by irreversibly blocking platelets, the compounds found in blood responsible for clotting after an injury or during a heart attack. However, these effects also place patients at increased risk for bleeding after coronary artery bypass surgery. Therefore, it is currently recommended to withhold Plavix therapy for 5 days before undergoing surgery in order to reduce the incidence of bleeding. However, it has been repeatedly shown that Plavix exerts variable effects on different patients, which may be partially explained by poor absorption, drug-drug interaction, and by variations in deoxyribonucleic acid (DNA) which constitutes your genes. In addition, the time required for platelets to regain function after Plavix treatment has been shown to vary between patients. Therefore, by measuring platelet function, it may be possible to determine the optimal amount of time required to withhold Plavix before undergoing bypass surgery, which may improve rates of bleeding following the procedure. The purpose of this study is to classify patients into groups based on platelet function in order to define the ideal time period for delaying surgery. By analyzing the amount of time required for platelet recovery, it is expected that surgery-related bleeding will decrease without increasing the risk of blood clot formation. Eligibility: Approximately 200 patients requiring CABG will be enrolled at Sinai Hospital, which is the only site where this study is being conducted. To be eligible you must: Be able to provide written informed consent. Be between the ages of 18-85 and require CABG. Currently be on aspirin therapy (81-325mg).
Detailed Description
Primary objective: We hypothesize that stratifying patients on clopidogrel into time-based platelet function recovery groups as determined by pre-operative clopidogrel response measured by point of care methods will result in similar rates of bleeding as compared to those of clopidogrel naïve patients undergoing elective CABG. Study design: This will be a single center, prospective study analyzing clopidogrel naïve patients and patients on clopidogrel with background aspirin therapy requiring CABG.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Coronary Artery Disease, CABG, Clopidogrel, Aspirin, Point of Care devices

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aspirin only
Arm Type
No Intervention
Arm Description
Continue aspirin until surgery
Arm Title
Clopidogrel and Aspirin
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
Clopidogrel withdraw prior to CABG
Intervention Description
Patients on clopidogrel are stratified into time-based platelet function recovery groups as determined by point of care methods and based on these groups clopidogrel is withdrawn at a pre-specified timepoint before surgery.
Primary Outcome Measure Information:
Title
The primary endpoint is chest tube drainage.
Time Frame
During the index hospitalization
Secondary Outcome Measure Information:
Title
The secondary endpoint is transfusion requirements.
Time Frame
Index hospitalization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must provide written informed consent. Patients must currently be on aspirin therapy (81-325 mg). Male or female patients between the ages of 18-85 requiring CABG. Exclusion Criteria: Patients undergoing emergent surgery following failed percutaneous coronary revascularization. Patients with a history of previous cardiac surgery and patients needing concomitant valvular surgery. Pre-operative exposure to either coumadin or platelet GPIIb/IIIa inhibitors. Patients with a history of bleeding diathesis. Patients with an activated partial thrombin time >1.5 normal. Patients with platelet count <120,000/mm3. Patients with hematocrit <30%. Patients with creatinine clearance <30mL/min. Patients with known active hepatic disease. Patients with any other condition that, in the opinion of the investigator, may either put the patient at risk or influence the result of the study (e.g. malignancy, limiting life expectancy, noncompliance).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kevin P Bliden, BS
Phone
4106014795
Email
kbliden@lifebridgehealth.org
First Name & Middle Initial & Last Name or Official Title & Degree
Paul P Gurbel, MD
Phone
4106019600
Email
pgurbel@lifebridgehealth.org
Facility Information:
Facility Name
Sinai Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kevin P Bliden

12. IPD Sharing Statement

Citations:
PubMed Identifier
22396581
Citation
Mahla E, Suarez TA, Bliden KP, Rehak P, Metzler H, Sequeira AJ, Cho P, Sell J, Fan J, Antonino MJ, Tantry US, Gurbel PA. Platelet function measurement-based strategy to reduce bleeding and waiting time in clopidogrel-treated patients undergoing coronary artery bypass graft surgery: the timing based on platelet function strategy to reduce clopidogrel-associated bleeding related to CABG (TARGET-CABG) study. Circ Cardiovasc Interv. 2012 Apr;5(2):261-9. doi: 10.1161/CIRCINTERVENTIONS.111.967208. Epub 2012 Mar 6.
Results Reference
derived

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Time Based Strategy to Reduce Clopidogrel Associated Bleeding Related to Coronary Artery Bypass Graft (CABG)

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