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NCT06878638Completed

Nitrate - Clopidogrel - Acute Coronary Syndrome

Impact of Intravenous Nitrate Treatment on Antiplatelet Effects of Clopidogrel in Acute Coronary Syndrome Patients: A Pilot Study

Source: ClinicalTrials.gov · Last updated 17 Mar 2025

Brief summary (registry, in English)

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

Status (registry)
Completed
Study type
Observational
Enrollment
20 (actual)
First submitted
5 Mar 2025
Start date
1 Feb 2023
Primary completion date
1 Jan 2024
Lead sponsor
Bursa Postgraduate Hospital
NCT number
NCT06878638

What you commit to

  • Study type: Observational
  • Participants enrolled: 20
  • From 1 Feb 2023 to the primary completion date, 1 Jan 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • use of narcotic analgesics (e.g., morphine), nitrates and glycoprotein IIb/IIIa inhibitors during hospitalization,

Other illness

  • recurrent angina,
  • 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),
  • allergy to ASA or clopidogrel, coagulopathy,

Lab values

  • left ventricular systolic dysfunction (ejection fraction \<50%),
  • platelet counts below 100,000/μl and hematocrit levels below 29%, or exceeding 52%.

Other

  • Hemodynamically unstable and requiring urgent intervention,
  • ST elevation on electrocardiography, atrial fibrillation,
  • glomerular filtration rate \<60 mL/min/1.73m2,

Who the study is looking for

  • diagnosed with non-STEMI
  • Patients aged 18 to 75 years
  • positive troponin levels,
  • blood pressure above 120/70 mmHg

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bursa Yüksek İhtisas Hastanesi
Coordinator of this site? Confirm its status
BursaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.