跳至主要内容
临床试验/CTRI/2018/04/013094
CTRI/2018/04/013094尚未招募未知

Safety and clinical effectiveness of Alteplase in acute ischemic stroke: An observational study in a tertiary care hospital.

Department of Pharmacolog0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • patients aged 18 to 80 years diagnosed with acute ischemic stroke and who has been administered Alteplase would be included.

排除标准

  • Those who are contraindicated for thrombolysis.

研究者

发起方
Department of Pharmacolog

相似试验

进行中(未招募)
不适用
A placebo controlled trial of alteplase (rt-PA) in acute ischemichemispheric stroke where thrombolysis is initiated between 3 and 4hours 30 minutes after stroke onset - ECASS IIIAcute ischemic hemispheric stroke
EUCTR2005-003176-38-CZBoehringer Ingelheim France800
进行中(未招募)
1 期
A placebo controlled trial of alteplase (rt-PA) in acute ischemic hemispheric stroke where thrombolysis is initiated between 3 and 4 hours 30 minutes after stroke onset - ECASS IIIAcute ischemic hemispheric stroke
EUCTR2005-003176-38-SKBoehringer Ingelheim France800
进行中(未招募)
不适用
A placebo controlled trial of alteplase (rt-PA) in acute ischemic hemispheric stroke where thrombolysis is initiated between 3 and 4 hours 30 minutes after stroke onset - ECASS IIIIschemic stroke 3 and 4 hours 30 minutes before treatment
EUCTR2005-003176-38-HUBoehringer Ingelheim Pharma Ges mbH800
已完成
1 期
Clinical studies on the safety and efficacy of platelet rich plasma used in anterior cruciate ligament reconstructiorupture of anterior cruciate ligament
JPRN-UMIN000014694niversity of tsukuba Department of Orthopaedic Surgery5
进行中(未招募)
不适用
A randomized controlled trial of alteplase (rt-PA) vs standard treatment in acute ischemic hemispheric stroke in patients aged more than 80 years where thrombolysis is initiated within 3 hours after stroke onset - NDacute ischemic strokeMedDRA version: 9.1Level: LLTClassification code 10043647Term: Thrombotic stroke
EUCTR2007-006177-88-ITAZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA
A study to observe the side effects and patient... | 临床试验