跳至主要内容
临床试验/EUCTR2007-005462-12-SE
EUCTR2007-005462-12-SE进行中(未招募)不适用

A prospective, randomized, masked and controlled trial of intravitreal ranibizumab (Lucentis®) combined with transpupillary thermotherapy (TTT) in patients with neovascular age-related macular degeneration (AMD)

St. Eriks Eye Hospital0 个研究点目标入组 100 人开始时间: 2007年10月15日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients with neovascular AMD age 50 years or older who have a visual acuity of 0.1 (20/200) or better
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients aged < 50 years
  • BCVA < 0.1
  • Subfoveal fibrosis or atrophy
  • Previous treatment for neovascular AMD
  • CNV of other causes that AMD
  • Intraocular surgery within 3 months
  • Untreated glaucoma
  • Inflammation or infection in study eye
  • Retinal vascular disease of any origin

研究者

发起方
St. Eriks Eye Hospital

相似试验

进行中(未招募)
不适用
A prospective, randomized, masked and controlled trial of intravitreal bevacizumab (Avastin®) for central retinal vein occlusion (CRVO).Central retinal vein occlusion (CRVO) is a sight-threatening ocular condition without efficient treatment.
EUCTR2008-006265-93-SESt Eriks Eye Hospital60
进行中(未招募)
不适用
A prospective, randomized, masked and controlled trial of intravitreal bevacizumab (Avastin) versus verteporfin photodynamic therapy (PDT) in patients with neovascular age-related macular degeneration.
EUCTR2006-001200-36-SESt. Eriks Eye Hospital100
招募中
不适用
A prospective clinical trial for the treatment of keratoconjunctivitis caused by microsporidia.
CTRI/2011/11/002132Hyderabad Eye Research Foundation72
进行中(未招募)
不适用
A prospective, controlled, randomized, patient and evaluator blinded study to evaluate pain and further disabling complications in patients undergoing Lichtenstein technique for primary inguinal hernia repair by fixing the mesh with TISSUCOL/TISSEEL fibrin sealant versus sutures. - TIMELI 001nilateral, uncomplicated primary inguinal hernia repairClassification code 10022020
EUCTR2005-002741-39-DKniversità di Milano, Dipartimento di Scienze Chirurgiche, Ospedale Maggiore Policlinico, Padiglione328
进行中(未招募)
1 期
A prospective, controlled, randomized, patient and evaluator blinded study to evaluate pain and further disabling complications in patients undergoing Lichtenstein technique for primary inguinal hernia repair by fixing the mesh with TISSUCOL/TISSEEL fibrin sealant versus sutures.
EUCTR2005-002741-39-ESPr Giampiero CAMPANELLI - Ospedale Maggiore Policlinico, Padiglione Beretta Est328