EUCTR2011-004025-27-AT进行中(未招募)不适用
Efficacy and safety of a fixed combination of cinnarizine 20 mg and dimenhydrinate 40 mg vs betahistine dihydrochloride 16 mg in patients with vertigo of peripheral origin. A multi-centre, double-blind, randomised, active-controlled, stratified two-parallel group clinical study
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 224
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
- •written Informed Consent of the patient
- •patient has vertigo sensations of peripheral-vestibular origin, e.g. Menière-like symptoms
- •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 178
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 46
排除标准
- •simultaneous participation in another clinical study
- •patient did not voluntarily sign the informed consent form
- •intake of antivertiginous or cerebrovascularly active medication that cannot be discontinued
- •known allergic reactions to one of the active substances of the study medication (cinnarizine, dimenhydrinate and/or betahistine dihydrochloride)
- •known hypersensitivity to various medicaments
- •suspicion of alcohol and/or drug abuse
- •psychiatric diseases, insanity
- •epilepsy or convulsive fits
- •acute infections
- •severe chronic or terminal diseases (cancer, tuberculosis)
- •any disease that could affect absorption, metabolism or elimination of the study medication
- •acute poisoning
- •suspected pregnancy / nursing period / women of child-bearing potential, if no safe contraception can be guaranteed during the study
- •chronic inflammatory middle ear diseases
- •Parkinson’s disease
- •suspected compressive intracranial processes
- •suspected narrow-angle glaucoma
- •suspected prostate adenoma with formation of residual urine in the bladder
- •severe renal insufficiency
- •chronic liver disease
- •treatment with aminoglycosidic antibiotics
- •treatment with monoaminooxidase inhibitors, tricyclic antidepressants, para-sympatholytics, glucocorticoids and/or heparin that cannot be discontinued
- •phaeochromocytoma
- •peptic ulcer
研究者
相似试验
进行中(未招募)
1 期
Efficacy and safety of a fixed combination of cinnarizine 20 mg and dimenhydrinate 40 mg vs betahistine dihydrochloride 16 mg in patients with inner ear vertigo.Vertigo of peripheral originMedDRA version: 16.1Level: LLTClassification code 10031615Term: Other and unspecified peripheral vertigoSystem Organ Class: 10013993 - Ear and labyrinth disordersMedDRA version: 16.1Level: LLTClassification code 10058708Term: Rotatory vertigoSystem Organ Class: 10013993 - Ear and labyrinth disordersMedDRA version: 16.1Level: PTClassification code 10047344Term: Vertigo labyrinthineSystem Organ Class: 10013993 - Ear and labyrinth disordersMedDRA version: 16.1Level: LLTClassification code 10034641Term: Peripheral vertigo, unspecifiedSystem Organ Class: 10013993 - Ear and labyrinth disordersMedDRA version: 16.1Level: LLTClassification code 10032379Term: Other peripheral vertigoSystem Organ Class: 10013993 - Ear and labyrinth disordersEUCTR2011-004025-27-BGHENNIG ARZNEIMITTEL GmbH & Co. KG224
进行中(未招募)
1 期
Efficacy and safety of a fixed combination of cinnarizine 20 mg and dimenhydrinate 40 mg vs betahistine dihydrochloride 16 mg in patients with inner ear vertigo.EUCTR2011-004025-27-CZHENNIG ARZNEIMITTEL GmbH & Co. KG306
进行中(未招募)
1 期
Efficacy and safety of a fixed combination of ciclesonide and formoterol once or twice daily in the treatment of persistent asthma A randomized, double-blind, placebo-controlled, parallel-group, multi-center study - EFFORTasthma bronchialeMedDRA version: 5.1Level: lltClassification code 10003553EUCTR2004-001838-16-CZALTANA Pharma AG810
进行中(未招募)
1 期
Efficacy and safety of a fixed combination of ciclesonide and formoterol once or twice daily in the treatment of persistent asthma A randomized, double-blind, placebo-controlled, parallel-group, multi-center study - EFFORTasthma bronchialeMedDRA version: 5.1Level: lltClassification code 10003553EUCTR2004-001838-16-HUALTANA Pharma AG810
已完成
不适用
Investigation on efficacy and safety of combination treatment with imidafenacin and mirabegron in patients with overactive bladder.overactive bladderJPRN-UMIN000016236Clinical Research Support Center Kyushu30
