DLBS1033 for Acute NSTEMI Without Early Coronary Revascularization
- Conditions
- Acute Non-ST Elevation Myocardial Infarction
- Interventions
- Drug: Placebo
- Registration Number
- NCT02146664
- Lead Sponsor
- Dexa Medica Group
- Brief Summary
This is a prospective, randomized, double-blind, double-dummy, and controlled study of DLBS1033 in the management of acute non-ST elevation myocardial infarction (NSTEMI) without early coronary revascularization. It is hypothesized that the combination of DLBS1033 with aspirin and clopidogrel will result in greater reduction of infarct size in comparison with that of aspirin and clopidogrel alone.
- Detailed Description
After diagnosed NSTEMI, patient is hospitalized and given medications according to the standard management of acute NSTEMI, including anticoagulant low molecular weight heparin. Eligible subjects are then randomized to receive either DLBS1033 at a dose of 490 mg three times daily or its placebo in addition to clopidogrel 75 mg once daily and aspirin 160 mg once daily for an 8-week course of therapy. Afterwards, the administration of DLBS1033 and its placebo are stopped, while the dual antiplatelet therapy (aspirin and clopidogrel) remains for another 16 weeks at the same dose regimen as the previous.
Clinical and laboratory examinations to evaluate the investigational drug's efficacy and safety are performed at baseline, week 4, week 8, and week 24. To guard the safety of the study subjects, haemostasis parameters, hematology parameters, and CRUSADE bleeding score are evaluated every two-week-interval over the first eight weeks of treatment.
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
-
Men and women of 30-75 years of age.
-
Evidence of acute non-ST elevation myocardial infarction (NSTEMI) at screening, as confirmed by all of the following:
- ECG transient ST-segment deviation/depression (≥ 1 mm) or prominent T-wave inversion, in multiple precordial leads;
- Positive plasma biomarkers of myocardial necrosis: cardiac troponin I (cTnI);
- Clinical symptoms of chest discomfort/pain or anginal equivalent (dyspnea, diaphoresis, excessive vomiting in diabetic patients and arm or jaw pain).
-
High risk subjects, defined as having Thrombolysis in Myocardial Infarction (TIMI) score ≥ 4
-
Subjects refuse to undergo reperfusion therapies, such as coronary artery-bypass surgery (CABG) or percutaneous coronary intervention (PCI) within the next six months.
-
Therapy with study medication can be started within 7 days after first presentation in the hospital.
-
Able to take oral medication.
- For females of childbearing potential: pregnancy, breast-feeding, the intention of becoming pregnant.
- ECG presentation of STEMI.
- History of hemorrhagic stroke within the last 3 months.
- Patients with seizure at the onset of stroke or with regular medication for seizure/epilepsy.
- History of serious head injury within the last 3 months.
- History of major surgery within the last 3 months.
- Ongoing long term need for oral anticoagulants, antiplatelets, fibrinolytic, or antithrombotic agents, other than the study medication.
- Having any implanted pacemaker or cardiac resynchronization therapy (CRT) or cardiac resynchronization therapy defibrillators (CRT-D).
- Clinically significant arrhythmias or atrioventricular conduction block greater than first degree.
- Acute or chronic heart failure as defined by the New York Heart Association (NYHA) classification as functional Class IV.
- Known severe LV dysfunction (EF ≤ 40 and EDD > 55 mm).
- Inadequate liver function: ALT > 3 times upper limit of normal (ULN).
- Inadequate renal function: serum creatinine ≥ 1.5 times upper limit of normal (ULN).
- Uncontrolled hypertension (SBP > 185 mmHg or DBP > 110 mmHg).
- Random plasma glucose ≥ 180 mg/dL and HbA1c ≥ 7.0% at Screening.
- Moderate to high risk of bleeding, defined as those who have the CRUSADE bleeding score of > 30.
- Known or suspected allergy to any of study medications used in the study, including other lumbrokinase products.
- Prior experience with DLBS1033 or other oral lumbrokinase products.
- Clinical evidence of malignancies with survival period < 1 year.
- Any other disease which judged by the investigator could interfere with trial participation or trial evaluation.
- Enrolled in other interventional protocol within 30 days prior to Screening.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo Placebo is administered one tablet three times daily, everyday for eight weeks of study period DLBS1033 DLBS1033 DLBS1033 enteric-coated tablet is administered at the dose of 490 mg, one tablet three times daily, everyday for eight weeks of study period
- Primary Outcome Measures
Name Time Method Infarct size Week 0, week 8, week 24 The quantitative change of infarct size, measured using SPECT.
- Secondary Outcome Measures
Name Time Method Routine hematology Week 0, 4, 8, and 24 Routine hematology measured includes: hemoglobin, hematocrit, RBC, WBC, differentiation of WBC, and platelet count. Particularly for hemoglobin and hematocrit level, they are measured at baseline and every interval of 2 weeks over the first 8 weeks of treatment and at the end of study (week 24).
Liver function Week 0, 4, 8, and 24 Liver function measured includes: serum ALT (SGPT), serum AST (SGOT), alkaline phosphatase, and total bilirubin. Particularly for serum ALT, it is measured at baseline and every interval of 2 weeks over the first 8 weeks of treatment and at the end of study (week 24).
Adverse event Week 0 - 24 Adverse events (especially major and minor bleeding) are observed and carefully evaluated along the course of the study.
LV function Week 0, week 4, week 8, and week 24 Improvement in left ventricular (LV) function, measured by 2D echocardiography.
Renal function Week 0, 4, 8, and 24 Renal function measured includes: serum creatinine and BUN. Particularly for serum creatinine, it is measured at baseline and every interval of 2 weeks over the first 8 weeks of treatment and at the end of study (week 24).
Haemostasis parameter Week 0, 4, 8, and 24 Haemostasis parameter measured includes: prothrombin time (PT), International Normalized Ratio (INR), and activated partial thromboplastin time (aPTT). Particularly for PT and INR, they are measured at baseline and every interval of 2 weeks over the first 8 weeks of treatment and at the end of study (week 24).
Composite endpoints Week 0 - 24 Composite endpoints (composite of major adverse cardiovascular events), comprising of all-cause of death, recurrent myocardial infarction or ischemic stroke within the study period.
Nitroglycerin amount Week 0 - 24 Number of nitroglycerin (rescue medicine) taken during the study period.
Plasma fibrinogen level Week 0, 4, 8, and 24 Change in plasma fibrinogen level.
Plasma d-dimer level Week 0, 4, 8, and 24 Change in plasma d-dimer level.
hs-CRP Week 0, 4, 8, and 24 Change in hs-CRP.
Individual event of MACE and other cardiovascular events Week 0 - 24 Individual event of MACE and other cardiovascular events, such as: shock, pulmonary oedema, congestive heart failure, arrhythmias, hemodynamic instability/cardiogenic shock, including the presence of new infarct(s) within the study period.
Trial Locations
- Locations (2)
Binawaluya Cardiac Hospital
🇮🇩Jakarta, Indonesia
Central Army Hospital RSPAD Gatot Soebroto
🇮🇩Central Jakarta, Jakarta, Indonesia