跳至主要内容
临床试验/CTRI/2009/091/000651
CTRI/2009/091/000651招募中2 期

A Randomized, Double-Blind, Double-Dummy, Paralle Group Study to Compare YM150 bid and qd Doses and Enoxaparin for Prevention of Venous Thromboembolism in Subjects Undergoing Elective Hip Replacement Surgery.Acronym: ONYX-3

Astellas Pharma Inc.0 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
2 期
状态
招募中

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

入选标准

  • Male or female subject aged 18 years or older.
  • Subject is scheduled for elective hip replacement surgery.

排除标准

  • - Subject has active bleeding or any condition associated with increased risk of bleeding
  • - Subject has had major trauma or surgery within 3 months before planned hip replacement surgery or requires major surgery or other invasive procedures with potential for uncontrolled bleeding during the study
  • - Subject has had an MI or stroke within 3 months before planned hip replacement surgery

研究者

相似试验

进行中(未招募)
1 期
A Randomised, Double-Blind, Double-Dummy, Parallel Group Comparison of 24 Weeks of Treatment with Ropinirole Immediate Release (IR) Tablets or Ropinirole Prolonged Release / Extended Release (PR/XR) Tablets in Advanced Stage Parkinson’s Disease Subjects who are not Adequately Controlled on L-dopa.Parkinson's disease
EUCTR2005-005423-34-GBGlaxoSmithKline Research & Development Ltd
进行中(未招募)
不适用
A Randomised, Double-Blind, Double-Dummy, Parallel Group Comparison of 24 Weeks of Treatment with Ropinirole Immediate Release IR Tablets or Ropinirole Prolonged Release / Extended Release PR/XR Tablets in Advanced Stage Parkinson s Disease Subjects who are not Adequately Controlled on L-dopa. - NDParkinson diseaseMedDRA version: 6.1Level: PTClassification code 10061536
EUCTR2005-005423-34-ITGlaxoSmithKline R D516
进行中(未招募)
不适用
A Randomised, Double-Blind, Double-Dummy, Parallel-Group, Placebo-Controlled, Forced Dose Titration Study Evaluating the Efficacy and Safety of GW679769 and Paroxetine in Subjects with Major Depressive DisorderMajor Depressive DisordersMedDRA version: 9.1Level: LLTClassification code 10057840Term: Major depression
EUCTR2004-004984-32-ITGLAXO SMITHKLINE500
进行中(未招募)
不适用
A Randomised, Double-Blind, Double-Dummy, Parallel-Group, Placebo-Controlled, Forced Dose Titration Study Evaluating the Efficacy and Safety of GW679769 and Paroxetine in Subjects with Major Depressive Disorder
EUCTR2004-004984-32-SEGlaxoSmithKline Research and Development Limited348
已完成
3 期
A Randomised, Double-Blind, Double-Dummy, Parallel-Group, Multicentre Study to assess efficacy and safety of Fluticasone Furoate (FF)/GW642444 Inhalation Powder and Fluticasone Propionate FP)/Salmeterol Inhalation Powder in the Treatment of Persistent Asthma in Adults and Adolescents.Persistent Asthma10006436Asthma
NL-OMON34054GlaxoSmithKline62