PER-008-16已完成未知
A PHASE III, RANDOMIZED, INTERNATIONAL, MULTICENTER, OPEN LABEL, WITH BLINDED ADJUDICATION OF OUTCOMES, NON-INFERIORITY CLINICAL TRIAL TO EXPLORE THE SAFETY AND EFFICACY OF TICAGRELOR COMPARED WITH CLOPIDOGREL IN PATIENTS WITH ST ELEVATION MYOCARDIAL INFARCTION TREATED WITH PHARMACOLOGICAL THROMBOLYSIS
Associação do Sanatorio Sirio – Hospital do Coração,0 个研究点目标入组 32 人开始时间: 2016年8月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 32
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 75(—)
- 性别
- All
入选标准
- •Patients with a diagnosis of acute coronary syndrome with ST elevation with onset during the previous 24 hours, documented by cardiac ischemic symptoms due to atherosclerosis of > 10 minutes duration at rest, treated with pharmacological thrombolysis.
- •Both male and female, aged ≥ 18 years and < 75 years
- •Agreement to provide written informed consent
排除标准
- •any contraindication against the use of clopidogrel or ticagrelor (eg, hypersensitivity, moderate or severe liver disease, active bleeding or recent bleeding history, history of intracranial hemorrhage)
- •need for oral anticoagulation therapy, or aspirin doses per day more than 100mg/day.
- •concomitant oral or IV therapy with strong CYP3A inhibitors (ketoconazole, itraconazole, voriconazole, telithromycin, clarithromycin, nefazodone, ritonavir, saquinavir, nelfinavir, indinavir, atazanavir, grapefruit juice N1 L/d), CYP3A substrates with narrow therapeutic indices (cyclosporine, quinidine), or strong CYP3Ainducers (rifampin/rifampicin, phenytoin, carbamazepine)
- •Increased risk of bradyarrithmias
- •Dialysis required
- •Known clinically important thrombocytopenia
- •Known clinically important anemia
- •Any other condition that may put the patient at risk or influence study results in the investigators´ opinion (eg, cardiogenic shock, severe hemodynamic instability, active cancer)
- •Participant in another investigational drug or device study within 30 d
- •Current use of Ticagrelor
- •Pregnancy or lactation
- •Any condition that increases the risk for noncompliance or being lost to follow-up
- •Involvement in the planning or conduct of the study
- •Previous enrollment or randomization in this study
- •Contraindications to fibrinolytic therapy
研究者
相似试验
进行中(未招募)
1 期
Trial to evaluate the analgesic efficacy and safety of ibuprofen arginine/tramadol compared with ibuprofen alone and placebo, in patients with moderate to severe pain after non-oncological abdominal hysterectomy.Evaluation of the analgesic efficacy in patients with moderate to severe pain after non-oncological abdominal surgery.MedDRA version: 17.1Level: PTClassification code 10021151Term: HysterectomySystem Organ Class: 10042613 - Surgical and medical proceduresEUCTR2014-004081-21-ESaboratorios Farmalíder S.A.444
进行中(未招募)
不适用
Trial to evaluate the analgesic efficacy and safety of ibuprofen arginine/tramadol compared with ibuprofen alone and placebo, in patients with moderate to severe pain after non-oncological abdominal hysterectomy.Evaluation of the analgesic efficacy in patients with moderate to severe pain after non-oncological abdominal surgery.MedDRA version: 17.1Level: PTClassification code 10021151Term: HysterectomySystem Organ Class: 10042613 - Surgical and medical proceduresEUCTR2014-004081-21-HUaboratorios Farmalíder S.A.444
进行中(未招募)
1 期
A Study to Evaluate the Efficacy and Safety of Obinutuzumab Versus Mycophenolate Mofetil (MMF) in Patients with Childhood Onset Idiopathic Nephrotic SyndromeChildhood Onset Idiopathic Nephrotic SyndromeMedDRA version: 21.1Level: PTClassification code 10029164Term: Nephrotic syndromeSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2022-000369-42-BEF. Hoffman-La Roche Ltd.80
招募中
3 期
A phase III trial of RO5072759 in childhood onset idiopathic nephrotic syndrome patientsChildhood Nephrotic SyndromeJPRN-jRCT2011220036Will Pendergraft, M.D., Ph.D.80
进行中(未招募)
1 期
A Study to Evaluate the Efficacy and Safety of Obinutuzumab Versus Mycophenolate Mofetil (MMF) in Patients with Childhood Onset Idiopathic Nephrotic SyndromeChildhood Onset Idiopathic Nephrotic SyndromeMedDRA version: 21.1Level: PTClassification code 10029164Term: Nephrotic syndromeSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2022-000369-42-PLF. Hoffman-La Roche Ltd80
