Coronary Artery Disease Clinical Trial
Official title:
Different Platelet Activities Between Intracoronary and Peripheral Blood in Coronary Artery Disease Patients
Antiplatelet treatment is important for coronary artery disease(CAD) patients .Some patients
are resistant to antiplatelet treatment based on platelet function tests(PFT).Currently the
results of PFT are mainly based on the analysis of peripheral blood. instead, adverse
cardiovascular events in CAD patients may be more directly related to platelet activities in
the coronary arteries. There's no evidence of system study to prove the PFT of peripheral
blood can represent the platelet functions in coronary arteries.The purpose of this study is
to determine the different platelet activities in the blood of peripheral vein (PV),
peripheral artery (PA), intracoronary artery (IC) in the CAD patients without or with
different interventions.
our study is divided into three parts: Part A: To study the different platelet activities in
the blood of PV, PA, IC in the CAD patients with dual antiplatelet therapy.
Part B: To explore the different platelet activities of the above three sites in ST-segment
elevation myocardial infarction (STEMI) patients who are administrated platelet membrane
glycoprotein Ⅱb/Ⅲa (GPⅡb/Ⅲa) receptor antagonist ( tirofiban ) in PV or IC and dual
antiplatelet therapy.
Part C: To explore the different platelet activities of the above three sites in STEMI
patients who are administrated antiplatelet thrombolysin or placebo in PV and dual
antiplatelet therapy.
Part A:A total of 30 CAD patients are recruited.All patients are on loading dose of 300 mg
clopidogrel followed by a maintenance dose of 75 mg/d for at least 5 days and a loading dose
of 300 mg aspirin followed by a maintenance dose of 100 mg/d for at least 5 days. All
patients plan to receive coronary arteriography (CAG) or percutaneous coronary intervention
(PCI).The investigators sample blood from PV,PA and IC before PCI.Regional differences will
be compared between blood samples from PV,PA and IC by light aggregometry (agonists:
arachidonic acid, LTA-AA; adenosine diphosphat, LTA-ADP), VerifyNow P2Y12 assays.
Differences between LTA and VerifyNow P2Y12-assay will also be compared.
Part B:A total of 30 STEMI patients are recruited.Patients are randomly assigned to 2
groups.A group(n=15) is given tirofiban through PV, the other group(n=15) is given through
IC.All patients are on loading dose of 600 mg clopidogrel and 300 mg aspirin.All patients
plan to receive emergency PCI. Group PV: a loading dose of 10ug/kg tirofiban is given in 3
min through PV,followed by a maintenance dose of 0.15ug/kg*min for 48h.Group IC: a loading
dose of 10ug/kg tirofiban is given through IC,followed by a maintenance dose of
0.15ug/kg*min for 48h. Blood samples are collceted from PV, PA and IC before the injection
of loading dose tirofiban , and 15min after the injection.Regional differences will be
compared between blood samples from PV,PA and IC by LTA-AA; LTA-ADP,
LTA-RIS(agonists:ristocetin),VerifyNow P2Y12 assays.
Part C:A total of 30 STEMI patients are recruited.Patients are randomly assigned to 2
groups.A group(n=15) is given antiplatelet thrombolysin(the frist antiplatelet drugs based
on GP Ib receptor which completed the preclinical and phase I clinical studies,and already
has entered phase II clinical studies) through PV, the other group(n=15) is given placebo
through PV.All patients are on loading dose of 600 mg clopidogrel and 300 mg aspirin.All
patients plan to receive emergency PCI.Both Groups are given in the same way , a loading
dose of 5 IU/60kg in 5 min through PV,followed by a maintenance dose of 0.002 IU/kg/h for
48h. Blood samples are collceted from PV, PA and IC before the injection of loading dose of
antiplatelet thrombolysin or placebo, and 15 min after the injection.Regional differences
will be compared between blood samples from PV,PA and IC by LTA-AA; LTA-ADP, LTA-RIS and
VerifyNow P2Y12 assays.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT06030596 -
SPECT Myocardial Blood Flow Quantification for Diagnosis of Ischemic Heart Disease Determined by Fraction Flow Reserve
|
||
| Completed |
NCT04080700 -
Korean Prospective Registry for Evaluating the Safety and Efficacy of Distal Radial Approach (KODRA)
|
||
| Recruiting |
NCT03810599 -
Patient-reported Outcomes in the Bergen Early Cardiac Rehabilitation Study
|
N/A | |
| Recruiting |
NCT06002932 -
Comparison of PROVISIONal 1-stent Strategy With DEB Versus Planned 2-stent Strategy in Coronary Bifurcation Lesions.
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
| Recruiting |
NCT04242134 -
Drug-coating Balloon Angioplasties for True Coronary Bifurcation Lesions
|
N/A | |
| Completed |
NCT04556994 -
Phase 1 Cardiac Rehabilitation With and Without Lower Limb Paddling Effects in Post CABG Patients.
|
N/A | |
| Recruiting |
NCT05846893 -
Drug-Coated Balloon vs. Drug-Eluting Stent for Clinical Outcomes in Patients With Large Coronary Artery Disease
|
N/A | |
| Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
| Recruiting |
NCT05023629 -
STunning After Balloon Occlusion
|
N/A | |
| Completed |
NCT04941560 -
Assessing the Association Between Multi-dimension Facial Characteristics and Coronary Artery Diseases
|
||
| Completed |
NCT04006288 -
Switching From DAPT to Dual Pathway Inhibition With Low-dose Rivaroxaban in Adjunct to Aspirin in Patients With Coronary Artery Disease
|
Phase 4 | |
| Completed |
NCT01860274 -
Meshed Vein Graft Patency Trial - VEST
|
N/A | |
| Recruiting |
NCT06174090 -
The Effect of Video Education on Pain, Anxiety and Knowledge Levels of Coronary Bypass Graft Surgery Patients
|
N/A | |
| Terminated |
NCT03959072 -
Cardiac Cath Lab Staff Radiation Exposure
|
||
| Completed |
NCT03968809 -
Role of Cardioflux in Predicting Coronary Artery Disease (CAD) Outcomes
|
||
| Recruiting |
NCT04566497 -
Assessment of Adverse Outcome in Asymptomatic Patients With Prior Coronary Revascularization Who Have a Systematic Stress Testing Strategy Or a Non-testing Strategy During Long-term Follow-up.
|
N/A | |
| Recruiting |
NCT05065073 -
Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
|
Phase 4 | |
| Completed |
NCT05096442 -
Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Korean Patients With Coronary De Novo Lesions
|
N/A |