Optimized Antithrombotic Therapy of Acute Myocardial Infarction With Left Ventricular Mural Thrombus
NCT03415386 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2020-02-11
Summary
A multi-center study will be done to explore the optimal regimen of antithrombotic therapy for acute myocardial infarction with left ventricular mural thrombus. The investigators will evaluate the different combinations of antiplatelet drugs and anticoagulants for at least one month, such as aspirin 100mg qd+clopidogrel 75mg qd+warfarin (INR1.8-2.2), aspirin 100mg qd+clopidogrel 75mg qd+dabigatran 110mg bid, aspirin 100mg qd+ticagrelor 60mg bid+warfarin (INR1.8-2.2), and aspirin 100mg qd+ticagrelor 60mg bid+dabigatran 110mg bid. Transthoracic two-dimensional echocardiography will be done at the 1-month, 3-month and 6-month follow-ups to evaluate the left ventricular mural thrombus and determinate whether the antithrombotic therapy regimen could be regulated to double antiplatelet or anticoagulant+clopidogrel 75mg qd/ticagrelor 60mg bid. Then the investigators will complete the 12-month follow-up to evaluate the efficacy and safety of the optimal antithrombotic therapy regimen for acute myocardial infarction with left ventricular mural thrombus.
Conditions
- Acute Myocardial Infarction
- Left Ventricular Thrombus
Interventions
- DRUG
-
Combination of antiplatelet drugs and anticoagulants for at least one month
Combination of antiplatelet drugs and anticoagulants for at least one month, such as aspirin100mg qd+clopidogrel75mg qd+warfarin (INR1.8-2.2), aspirin100mg qd+clopidogrel75mg qd+dabigatran110mg bid, aspirin100mg qd+ticagrelor60mg bid+warfarin (INR1.8-2.2), and aspirin100mg qd+ticagrelor60mg bid+dabigatran110mg bid. Transthoracic two-dimensional echocardiography will be done at the 1-month, 3-month and 6-month follow-ups to evaluate the left ventricular mural thrombus and determinate whether the antithrombotic therapy regimen could be regulated to double antiplatelet or anticoagulant+clopidogrel75mg qd/ticagrelor60mg bid.
Sponsors & Collaborators
-
The First Affiliated Hospital with Nanjing Medical University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 20 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-06-30
- Primary Completion
- 2020-12-31
- Completion
- 2022-06-30
More Related Trials
-
1-month vs 12-month DAPT for ACS Patients Who Underwent PCI Stratified by IVUS: IVUS-ACS and ULTIMATE-DAPT Trials
NCT03971500 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Treatment of Post-STEMI Left Ventricular Thrombus With Optimized Anticoagulant
NCT03764241 ·Status: UNKNOWN ·Phase: PHASE3
-
EmploYEd Antithrombotic Therapies in Patients With Acute Coronary Syndromes HOspitalized in iTalian CCUs
NCT06316128 ·Status: COMPLETED
-
Bivalirudin in Elderly Patients With Acute ST-segment Elevation Myocardial Infarction
NCT03882775 ·Status: UNKNOWN ·Phase: PHASE4
-
Study Evaluating How Patients With Acute Coronary Syndrome Are Managed During 2 Years After Discharge
NCT01171404 ·Status: COMPLETED
-
Safety and Effectiveness of Intra-coronary Nitrite in Acute Myocardial Infarction
NCT01584453 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of Bivalirudin During Short-term Intervention of Non-infarction Related Artery After PPCI of STEMI
NCT04475835 ·Status: UNKNOWN ·Phase: NA
-
Dual Therapy With Dabigatran/Ticagrelor Versus Dual Therapy With Dabigatran/Clopidogrel in ACS Patients With Indication for NOAC Undergoing PCI
NCT04688723 ·Status: UNKNOWN ·Phase: PHASE4
-
COlchicine for Left VEntricular Remodeling Treatment in Acute Myocardial Infarction
NCT03156816 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of Low-dose Intracoronary Thrombolytic Therapy in STEMI (Heart Attack) Patients.
NCT03998319 ·Status: RECRUITING ·Phase: PHASE3
-
Evaluate Early Invasive Strategy for Patients With STEMI Presenting 24-48 Hours From Symptom Onset
NCT04962178 ·Status: UNKNOWN ·Phase: NA
-
Optimized Antiplatelet Therapy in Patients With CHD After Implantation of NeoVas™ BRS System
NCT04995159 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Comparison Of Reduced DAPT Followed by P2Y12 Inhibitor Monotherapy With Prasugrel vs stAndard Regimen in STEMI Patients
NCT05491200 ·Status: RECRUITING ·Phase: PHASE4
-
Targeting Investigation and Treatment in Patients With Type 2 Myocardial Infarction
NCT05419583 ·Status: COMPLETED ·Phase: NA
-
Compare Early With Deferred Invasive Strategy for STEMI Presenting 24-48 Hours From Symptom Onset
NCT04575012 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Antiplatelet Therapy After Successful Percutaneous Coronary Intervention for Chronically Occluded Coronary Artery
NCT06175377 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Effect of Low-dose Intracoronary Reteplase on Myocardial Infarct Size During Primary Percutaneous Coronary Intervention
NCT04571580 ·Status: TERMINATED ·Phase: PHASE3
-
CardiOvascular Risk and idEntificAtion of Potential High-risk Population in Acute Myocardial Infarction II (COREA-AMI II)
NCT02806102 ·Status: UNKNOWN
-
Efficacy Study of Combined Prasugrel and Bivalirudin Versus Clopidogrel and Heparin in Myocardial Infarction
NCT00976092 ·Status: UNKNOWN ·Phase: PHASE4
-
DLBS1033 for Acute NSTEMI Without Early Coronary Revascularization
NCT02146664 ·Status: WITHDRAWN ·Phase: PHASE2/PHASE3
-
Safety and Efficacy of Percutaneous Coronary Intervention Combined With Thrombolysis at Different Time
NCT03137212 ·Status: UNKNOWN ·Phase: NA
-
A Clinical Trials of Quick-Acting Heart Reliever for Moderate Coronary Stenosis
NCT01513070 ·Status: COMPLETED ·Phase: PHASE4
-
The Stabilization Of pLaques usIng Darapladib-Thrombolysis In Myocardial Infarction 52 Trial
NCT01000727 ·Status: COMPLETED ·Phase: PHASE3
-
Early Mineralocorticoid Receptor Antagonist Treatment to Reduce Myocardial Infarct Size
NCT01882179 ·Status: COMPLETED ·Phase: PHASE3
-
Rivaroxaban vErsus Warfarin for Antithrombotic TheRapy in Patients With LeFt Ventricular Thrombus After Acute STEMI
NCT05705089 ·Status: COMPLETED ·Phase: PHASE3