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Nitrate - Clopidogrel - Acute Coronary Syndrome

Completed
Conditions
Acute Coronary Syndromes
Registration Number
NCT06878638
Lead Sponsor
Bursa Postgraduate Hospital
Brief Summary

This study aims to investigate whether intravenous nitrate given during non-ST-elevation myocardial infarction (non-STEMI) affects the platelet inhibition of clopidogrel.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • diagnosed with non-STEMI
  • Patients aged 18 to 75 years
  • positive troponin levels,
  • blood pressure above 120/70 mmHg
Exclusion Criteria
  • Hemodynamically unstable and requiring urgent intervention,
  • ST elevation on electrocardiography, atrial fibrillation,
  • recurrent angina,
  • use of narcotic analgesics (e.g., morphine), nitrates and glycoprotein IIb/IIIa inhibitors during hospitalization,
  • history of coronary artery bypass graft (CABG) surgery,
  • active infection,
  • uncontrolled hypertension,
  • diabetes, cerebrovascular accident, Use P2Y12 inhibitor, proton pump inhibitor, oral anticoagulant, statin, CYP enzyme-inducing or inhibiting drugs at the time of admission,
  • active systemic disease (e.g., malignancy, thyroid disorders chronic inflammatory diseases, liver dysfunction),
  • left ventricular systolic dysfunction (ejection fraction <50%),
  • glomerular filtration rate <60 mL/min/1.73m2,
  • allergy to ASA or clopidogrel, coagulopathy,
  • platelet counts below 100,000/μl and hematocrit levels below 29%, or exceeding 52%.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Platelet Reactivity Unit level48 hours

Platelet Reactivity Unit \<208

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Bursa Yüksek İhtisas Hastanesi

🇹🇷

Bursa, Turkey

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