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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00857155
Acronym
TARGET-CABG
Enrollment
200
Registered
2009-03-06
Start date
2009-01-31
Completion date
2011-02-28
Last updated
2009-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Keywords

Coronary Artery Disease, CABG, Clopidogrel, Aspirin, Point of Care devices

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.

Interventions

OTHERClopidogrel withdraw prior to CABG

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.

Sponsors

LifeBridge Health
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frame
The primary endpoint is chest tube drainage.During the index hospitalization

Secondary

MeasureTime frame
The secondary endpoint is transfusion requirements.Index hospitalization

Countries

United States

Contacts

Primary ContactKevin P Bliden, BS
kbliden@lifebridgehealth.org4106014795
Backup ContactPaul P Gurbel, MD
pgurbel@lifebridgehealth.org4106019600

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026