ticlopidine has been researched along with Non-ST-Elevation Myocardial Infarction in 11 studies
Ticlopidine: An effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.
ticlopidine : A thienopyridine that is 4,5,6,7-tetrahydrothieno[3,2-c]pyridine in which the hydrogen attached to the nitrogen is replaced by an o-chlorobenzyl group.
Excerpt | Relevance | Reference |
---|---|---|
"The Targeted Platelet Inhibition to Clarify the Optimal Strategy to Medically Manage Acute Coronary Syndromes trial enrolled 9326 participants with ACS, who received aspirin plus clopidogrel or prasugrel." | 9.22 | Ascertainment, classification, and impact of neoplasm detection during prolonged treatment with dual antiplatelet therapy with prasugrel vs. clopidogrel following acute coronary syndrome. ( Armstrong, PW; Beaven, AW; Blackwell, KL; Cyr, DD; Eckart, D; Fox, KA; Houterloot, L; Morse, MA; Ohman, EM; Onken, JE; Prabhakaran, D; Ready, NE; Roe, MT; Schulte, PJ; Strickler, JH; White, HD; Winters, KJ; Wiviott, SD; Zafar, SY; Zamoryakhin, D, 2016) |
"Ticagrelor can lower the resting heart rate of patients and cause bradyarrhythmias in the 12th month after PCI." | 7.83 | Ticagrelor vs. clopidogrel in non-ST-elevation acute coronary syndromes. ( Dong, C; Liu, X; Ren, C; Ren, Q; Zhang, X, 2016) |
"In 6763 medically managed non-ST-segment elevation ACS patients randomized in TRILOGY ACS (Targeted Platelet Inhibition to Clarify the Optimal Strategy to Medically Manage Acute Coronary Syndromes) (prasugrel versus clopidogrel), we examined relationships between categories of peak troponin/upper limit of normal (ULN) ratio within 48 hours of the index ACS event (≈4." | 5.24 | Relationship Between Peak Troponin Values and Long-Term Ischemic Events Among Medically Managed Patients With Acute Coronary Syndromes. ( Brown, EB; Cyr, DD; Goldstein, SA; Hamm, CW; Lüscher, TF; Neely, M; Newby, LK; Ohman, EM; Roe, MT; White, HD, 2017) |
"The Targeted Platelet Inhibition to Clarify the Optimal Strategy to Medically Manage Acute Coronary Syndromes trial enrolled 9326 participants with ACS, who received aspirin plus clopidogrel or prasugrel." | 5.22 | Ascertainment, classification, and impact of neoplasm detection during prolonged treatment with dual antiplatelet therapy with prasugrel vs. clopidogrel following acute coronary syndrome. ( Armstrong, PW; Beaven, AW; Blackwell, KL; Cyr, DD; Eckart, D; Fox, KA; Houterloot, L; Morse, MA; Ohman, EM; Onken, JE; Prabhakaran, D; Ready, NE; Roe, MT; Schulte, PJ; Strickler, JH; White, HD; Winters, KJ; Wiviott, SD; Zafar, SY; Zamoryakhin, D, 2016) |
"Ticagrelor can lower the resting heart rate of patients and cause bradyarrhythmias in the 12th month after PCI." | 3.83 | Ticagrelor vs. clopidogrel in non-ST-elevation acute coronary syndromes. ( Dong, C; Liu, X; Ren, C; Ren, Q; Zhang, X, 2016) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 10 (90.91) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
Patel, A | 1 |
Goodman, SG | 2 |
Tan, M | 1 |
Suskin, N | 1 |
McKelvie, R | 1 |
Mathew, AL | 1 |
Lutchmedial, S | 2 |
Dehghani, P | 2 |
Lavoie, AJ | 1 |
Huynh, T | 1 |
Lavi, S | 2 |
Philipp, R | 1 |
Khan, R | 1 |
Yan, AT | 1 |
Radhakrishnan, S | 1 |
Sedlak, T | 1 |
Brunner, N | 1 |
Kim, HH | 1 |
Cieza, T | 2 |
Kassam, S | 1 |
Fordyce, CB | 1 |
Heffernan, M | 1 |
Jedrzkiewicz, S | 1 |
Madan, M | 1 |
Ahmed, S | 1 |
Barry, C | 1 |
Dery, JP | 2 |
Bagai, A | 1 |
Goldstein, SA | 1 |
Newby, LK | 1 |
Cyr, DD | 2 |
Neely, M | 1 |
Lüscher, TF | 1 |
Brown, EB | 1 |
White, HD | 4 |
Ohman, EM | 4 |
Roe, MT | 4 |
Hamm, CW | 1 |
Kern, A | 1 |
Gil, RJ | 1 |
Bojko, K | 1 |
Sienkiewicz, E | 1 |
Januszko-Giergielewicz, B | 1 |
Górny, J | 1 |
Bil, J | 1 |
Castini, D | 1 |
Persampieri, S | 1 |
Cazzaniga, S | 1 |
Ferrante, G | 1 |
Centola, M | 1 |
Lucreziotti, S | 1 |
Salerno-Uriarte, D | 1 |
Sponzilli, C | 1 |
Carugo, S | 1 |
Ren, Q | 1 |
Ren, C | 1 |
Liu, X | 1 |
Dong, C | 1 |
Zhang, X | 2 |
Eckart, D | 1 |
Schulte, PJ | 1 |
Morse, MA | 1 |
Blackwell, KL | 1 |
Ready, NE | 1 |
Zafar, SY | 1 |
Beaven, AW | 1 |
Strickler, JH | 1 |
Onken, JE | 1 |
Winters, KJ | 2 |
Houterloot, L | 1 |
Zamoryakhin, D | 1 |
Wiviott, SD | 1 |
Prabhakaran, D | 3 |
Fox, KA | 3 |
Armstrong, PW | 3 |
Kagawa, Y | 1 |
Shiode, N | 1 |
Kawase, T | 1 |
Tamekiyo, H | 1 |
Okimoto, T | 1 |
Hayashi, Y | 1 |
Hagström, E | 1 |
Hafley, G | 1 |
Neely, ML | 1 |
Sidhu, MS | 1 |
Boden, WE | 1 |
Wang, L | 1 |
Bi, Y | 1 |
Cao, M | 1 |
Ma, R | 1 |
Wu, X | 1 |
Zhang, Y | 2 |
Ding, W | 1 |
Liu, Y | 1 |
Yu, Q | 1 |
Jiang, H | 1 |
Sun, Y | 1 |
Tong, D | 1 |
Guo, L | 1 |
Dong, Z | 1 |
Tian, Y | 1 |
Kou, J | 1 |
Shi, J | 1 |
Cornel, JH | 1 |
Neely, B | 1 |
Jakubowski, JA | 1 |
Bhatt, DL | 1 |
Ardissino, D | 1 |
Erlinge, D | 1 |
Tantry, US | 1 |
Gurbel, PA | 1 |
Mehta, SR | 1 |
Fisher, HN | 1 |
Zhu, YE | 1 |
Welsh, RC | 1 |
Henderson, MA | 1 |
Siega, AJ | 1 |
Cheema, AN | 1 |
Wong, BY | 1 |
Kokis, A | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Comparison of Prasugrel and Clopidogrel in Acute Coronary Syndrome Subjects With Unstable Angina/Non-ST-Elevation Myocardial Infarction Who Are Medically Managed[NCT00699998] | Phase 3 | 9,326 participants (Actual) | Interventional | 2008-06-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The percentage of participants is the total number of participants experiencing an all-cause death, nonfatal MI, or nonfatal stroke divided by number of participants in the treatment arm. Endpoint events were adjudicated by the Clinical Endpoint Committee. (NCT00699998)
Timeframe: Randomization through end of study (30-month visit)
Intervention | percentage of participants with an event (Number) |
---|---|
Prasugrel: <75 Years of Age | 10.61 |
Prasugrel: 75 Years of Age or Older | 27.04 |
Clopidogrel: <75 Years of Age | 11.12 |
Clopidogrel: 75 Years of Age or Older | 26.83 |
The percentage of participants is the total number of participants experiencing a CV death, nonfatal MI, or nonfatal stroke divided by number of participants in the treatment arm multiplied by 100. Endpoint events were adjudicated by the Clinical Endpoint Committee. (NCT00699998)
Timeframe: Randomization through end of study (30-month visit)
Intervention | percentage of participants with an event (Number) |
---|---|
Prasugrel: <75 Years of Age | 10.06 |
Prasugrel: 75 Years of Age or Older | 24.64 |
Clopidogrel: <75 Years of Age | 10.96 |
Clopidogrel: 75 Years of Age or Older | 24.13 |
The percentage of participants is the total number of participants experiencing a CV death or nonfatal MI divided by number of participants in the treatment arm. Endpoint events were adjudicated by the Clinical Endpoint Committee. (NCT00699998)
Timeframe: Randomization through end of study (30-month visit)
Intervention | percentage of participants with an event (Number) |
---|---|
Prasugrel: <75 Years of Age | 9.61 |
Prasugrel: 75 Years of Age or Older | 22.53 |
Clopidogrel: <75 Years of Age | 10.21 |
Clopidogrel: 75 Years of Age or Older | 22.69 |
The percentage of participants is the total number of participants experiencing a CV death, nonfatal MI, nonfatal stroke or re-hospitalization for a recurrent UA divided by number of participants in the treatment arm. Endpoints events were adjudicated by the Clinical Endpoint Committee. (NCT00699998)
Timeframe: Randomization through end of study (30-month visit)
Intervention | percentage of participants with an event (Number) |
---|---|
Prasugrel: <75 Years of Age | 12.13 |
Prasugrel: 75 Years of Age or Older | 26.27 |
Clopidogrel: <75 Years of Age | 12.83 |
Clopidogrel: 75 Years of Age or Older | 25.67 |
Brain natriuretic peptide (BNP) is secreted by the ventricles of the heart in response to hemodynamic stress and is a biomarker associated with increased CV risk. Results are presented as geometric least squares means (Geometric LS means). Geometric LS means were adjusted for treatment + baseline value + clopidogrel status at randomization. (NCT00699998)
Timeframe: Day 30 and 6 Months
Intervention | picograms per milliliter (pg/mL) (Geometric Mean) | |
---|---|---|
Day 30 | 6 Months (n=725, 125, 701, 174) | |
Clopidogrel: <75 Years of Age | 319.345 | 250.982 |
Clopidogrel: 75 Years of Age or Older | 951.359 | 722.750 |
Prasugrel: <75 Years of Age | 313.494 | 253.434 |
Prasugrel: 75 Years of Age or Older | 1082.396 | 770.132 |
C-Reactive Protein (CRP) is a biomarker associated with inflammation and increased CV risk. Results are presented as geometric least squares means (Geometric LS means). Geometric LS means were adjusted for treatment + baseline value + clopidogrel status at randomization. (NCT00699998)
Timeframe: Day 30 and Month 6
Intervention | milligrams per liter (mg/L) (Geometric Mean) | |
---|---|---|
Day 30 | 6 Months (n=755, 143, 745, 178) | |
Clopidogrel: <75 Years of Age | 2.287 | 2.149 |
Clopidogrel: 75 Years of Age or Older | 2.226 | 1.543 |
Prasugrel: <75 Years of Age | 2.330 | 2.272 |
Prasugrel: 75 Years of Age or Older | 2.441 | 1.593 |
Seattle Angina Questionnaire (SAQ) is a validated, disease-specific questionnaire containing 11 questions (Q) yielding 5 summary scales related to angina: physical limitations, angina stability, angina frequency, treatment satisfaction and disease perception. In this study only angina frequency and the physical limitations scales were assessed. Anginal Frequency was assessed using Q3 and Q4 which consists of a Likert scale ranging from 1 to 6 (higher values equals better quality of life) to assess how often a patient is having symptoms now. Physical limitations was assessed using Q1 which contains 9 items each assessed via Likert scale ranging from 1 to 6 (higher values equals better quality of life) to assess how much a participant's condition is hampering their ability to do what they want to do. Scale scores are transformed to a 0-100 by subtracting the lowest possible score, dividing by the range of the scale, and multiplying by 100. Higher values equal better quality of life. (NCT00699998)
Timeframe: Baseline and follow-up (24 months)
Intervention | units on a scale (Mean) | |||
---|---|---|---|---|
Baseline, physical limitations | Baseline, angina frequency | 24 Months, physical limitations (n=420, 412) | 24 Months, angina frequency (n=420, 412) | |
Clopidogrel | 67.0 | 73.1 | 74.5 | 89.5 |
Prasugrel | 67.8 | 73.6 | 75.1 | 89.7 |
Variation in the genes encoding the cytochrome P450 (CYP) enzymes (CYP2C19) can reduce the ability to metabolize clopidogrel and a reduced platelet response and have been associated with increased rates of CV events including CV death. Participants were classified as extensive metabolizers (EM); reduced metabolizers (RM); or unknown (UNK) metabolizers based on their CYP2C19 genotype. Possible extensive metabolizer (EM) phenotypes include EM=extensive metabolizer, UM=ultra-rapid metabolizer, and EM (non-UM) that are not UM. Possible reduced metabolizer (RM) phenotypes include IM=intermediate metabolizer and PM=poor metabolizer. Genotypes associated with each predicted phenotype are presented; predicted phenotype is presented first followed by the genotype. Percentage=(number of participants with the predicted phenotype and genotype divided by the total number of participants per arm) multiplied by 100. (NCT00699998)
Timeframe: Baseline
Intervention | percentage participants with geneotype (Number) | ||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
UM, *1/*17 | UM, *17/*17 | EM (non-UM), *1/*1 | IM, *1/*2 | IM, *1/*3 | IM, *1/*4 | IM, *1/*6 | IM, *1/*8 | PM, *2/*2 | PM, *2/*3 | PM, *2/*4 | PM, *2/*6 | PM, *2/*8 | PM, *3/*3 | UNK, *1/*10 | UNK, *1/*13 | UNK, *1/*9 | UNK, *1/*9, *9/*17 | UNK, *13/*17 | UNK, *2/*13 | UNK, *2/*17 | UNK, *2/*9 | UNK, *3/*17 | UNK, *4/*17 | UNK, *4/*9 | UNK, *6/*17 | UNK, *8/*17 | UNK, *9/*17 | UNK, Undefined genotype | |
Clopidogrel: <75 Years of Age | 25.1 | 5.4 | 35.7 | 19.8 | 0.5 | 0.1 | 0.0 | 0.4 | 4.3 | 0.3 | 0.2 | 0.0 | 0.0 | 0.2 | 0.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 6.8 | 0.1 | 0.0 | 0.2 | 0.0 | 0.0 | 0.1 | 0.0 | 0.5 |
Clopidogrel: 75 Years of Age or Older | 21.8 | 4.3 | 41.2 | 19.7 | 0.6 | 0.3 | 0.2 | 0.3 | 3.8 | 0.3 | 0.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 6.2 | 0.0 | 0.3 | 0.0 | 0.0 | 0.2 | 0.0 | 0.0 | 0.6 |
Prasugrel: <75 Years of Age | 24.0 | 5.1 | 38.8 | 18.6 | 0.8 | 0.4 | 0.0 | 0.1 | 3.9 | 0.3 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.1 | 0.0 | 0.0 | 0.0 | 6.3 | 0.0 | 0.1 | 0.2 | 0.0 | 0.0 | 0.2 | 0.0 | 0.7 |
Prasugrel: 75 Years of Age or Older | 25.0 | 3.6 | 42.1 | 18.3 | 0.6 | 0.0 | 0.2 | 0.5 | 2.2 | 0.2 | 0.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.2 | 0.2 | 0.0 | 0.0 | 0.0 | 6.1 | 0.0 | 0.0 | 0.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.6 |
Platelet aggregation was measured by as measured by Accumetrics Verify Now™ P2Y12. Results were reported in P2Y12 Reaction Units (PRU). PRU represents the rate and extent of adenosine (ADP)-stimulated platelet aggregation. Lower values indicate greater P2Y12 platelet inhibition and lower platelet activity and aggregation. ANCOVA Model was used and values were corrected for treatment + baseline value + clopidogrel status at randomization. (NCT00699998)
Timeframe: Day 30 and 12 Months
Intervention | P2Y12 Reaction Units (PRU) (Least Squares Mean) | |
---|---|---|
Day 30 | Month 12 (n=386, 76, 400, 103) | |
Clopidogrel: <75 Years of Age | 193.489 | 199.003 |
Clopidogrel: 75 Years of Age or Older | 200.285 | 181.360 |
Prasugrel: <75 Years of Age | 93.280 | 94.529 |
Prasugrel: 75 Years of Age or Older | 151.872 | 135.096 |
All deaths, regardless of possible relatedness, with the exception of 1 event, were adjudicated by the Clinical Endpoint Committee (CEC) and are reported in this table. The 1 event which was not adjudicated was a result of the revocation of consent by the participant prior to their death. Deaths possibly related to study drug in the opinion of the investigator are also contained in the Serious Adverse Event (SAE) module. (NCT00699998)
Timeframe: Randomization through end of study (30-month visit)
Intervention | participants (Number) | |||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Congestive Heart Failure | Cardiogenic Shock | Cardiac Rupture | Myocardial Infarction | Dysrhythmia | Stent Thrombosis | Directly Related to Revascularization-CABG or PCI | Intracranial Hemorrhage | Non-Hemorrhagic Stroke | Sudden death due to cardiovascular event | Pulmonary Embolism | Stroke, unknown type | Other Cardiovascular Event | Cardiovascular event, unknown type | Accidental | Trauma | Hemorrhage, not intracranial | Infection | Malignancy | Suicide | Other Non-Cardiovascular event | Cause unknown (nonadjudicated event) | |
Clopidogrel: <75 Years of Age | 13 | 10 | 0 | 24 | 6 | 0 | 1 | 4 | 4 | 70 | 2 | 0 | 0 | 45 | 1 | 0 | 0 | 16 | 14 | 0 | 8 | 0 |
Clopidogrel: 75 Years of Age or Older | 23 | 9 | 0 | 21 | 3 | 0 | 1 | 1 | 3 | 43 | 1 | 0 | 1 | 45 | 1 | 1 | 4 | 17 | 11 | 0 | 6 | 0 |
Prasugrel: <75 Years of Age | 10 | 8 | 0 | 16 | 5 | 0 | 1 | 2 | 4 | 75 | 0 | 0 | 6 | 40 | 1 | 2 | 1 | 14 | 14 | 1 | 8 | 0 |
Prasugrel: 75 Years of Age or Older | 21 | 4 | 1 | 24 | 2 | 0 | 1 | 1 | 4 | 39 | 1 | 1 | 1 | 41 | 0 | 3 | 1 | 21 | 7 | 0 | 4 | 1 |
3 trials available for ticlopidine and Non-ST-Elevation Myocardial Infarction
8 other studies available for ticlopidine and Non-ST-Elevation Myocardial Infarction
Article | Year |
---|---|
Contemporary use of guideline-based higher potency P2Y12 receptor inhibitor therapy in patients with moderate-to-high risk non-ST-segment elevation myocardial infarction: Results from the Canadian ACS reflective II cross-sectional study.
Topics: Canada; Cross-Sectional Studies; Humans; Myocardial Infarction; Non-ST Elevated Myocardial Infarctio | 2021 |
Platelet distribution width as the prognostic marker in coronary bifurcation treatment.
Topics: Aged; Aspirin; Blood Platelets; Clopidogrel; Coronary Artery Disease; Drug-Eluting Stents; Female; H | 2017 |
Real-world clopidogrel utilization in acute coronary syndromes: patients selection and outcomes in a single-center experience.
Topics: Acute Coronary Syndrome; Adenosine; Aged; Aged, 80 and over; Chi-Square Distribution; Clopidogrel; D | 2017 |
Ticagrelor vs. clopidogrel in non-ST-elevation acute coronary syndromes.
Topics: Acute Coronary Syndrome; Adenosine; Bradycardia; Clopidogrel; Comorbidity; Electrocardiography; Fema | 2016 |
A case of subacute stent thrombosis after drug-coated balloon coronary angioplasty for in-stent restenosis under single anti-platelet therapy.
Topics: Aged; Angioplasty, Balloon, Coronary; Coronary Angiography; Coronary Restenosis; Coronary Vessels; D | 2017 |
Microparticles and blood cells induce procoagulant activity via phosphatidylserine exposure in NSTEMI patients following stent implantation.
Topics: Aged; Aspirin; Blood Cells; Blood Coagulation; Cell-Derived Microparticles; Clopidogrel; Female; Hum | 2016 |
Relationship of Platelet Reactivity With Bleeding Outcomes During Long-Term Treatment With Dual Antiplatelet Therapy for Medically Managed Patients With Non-ST-Segment Elevation Acute Coronary Syndromes.
Topics: Acute Coronary Syndrome; Aged; Angina, Unstable; Aspirin; Blood Platelets; Clopidogrel; Drug Therapy | 2016 |
Baseline characteristics, adenosine diphosphate receptor inhibitor treatment patterns, and in-hospital outcomes of myocardial infarction patients undergoing percutaneous coronary intervention in the prospective Canadian Observational AntiPlatelet sTudy (C
Topics: Adenosine; Adult; Aged; Aged, 80 and over; Canada; Clopidogrel; Drug Substitution; Emergency Medical | 2016 |