EUCTR2010-020122-18-FI进行中(未招募)不适用
A prospective, randomized, double-blind, double-dummy, placebo- and active controlled, multicenter study assessing the efficacy and safety of the combination BAY 60 4552 / vardenafil compared to vardenafil (20 mg) for the treatment of erectile dysfunction not sufficiently responsive to standard therapy with PDE5 inhibitors
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
- 267
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
- Male
入选标准
- •Open-label run-in phase (first four weeks)
- •Written informed consent signed before any study-specific procedure
- •History of ED for at least 6 months prior to screening, defined as the inability to achieve and maintain an erection of the penis sufficient to complete satisfactory sexual intercourse; the diagnosis of ED has to be confirmed by a physician
- •Stable, heterosexual relationship for at least 6 months prior to screening
- •Aged 18 to 64 years (inclusive) at the first screening examination
- •History of previous use of at least 1 marketed PDE5 inhibitor and insufficient therapeutic efficacy despite use of the highest approved dose
- •Double-blind treatment phase (last four weeks)
- •At least 4 attempts at sexual intercourse on 4 separate days during the open-label run-in phase with use of 20 mg vardenafil approximately 1 hour before attempting intercourse
- •IIEF EF score <17
- •At least 50% of attempts at sexual intercourse during the open-label run-in phase were unsuccessful
- •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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Contraindication to use of vardenafil
- •History of prostatectomy due to prostate cancer, including nerve-sparing techniques.
- •Concomitant use of adrenergic blockers
- •History of spinal cord injury
- •Resting hypotension, i.e. SBP <100 mmHg at rest
- •Moderate / severe hypertension, i.e. SBP >170 mmHg or DBP >110 mmHg at rest
- •Symptomatic orthostatic hypotension with a decrease in SBP >20 mmHg or in DBP >10 mmHg subsequent to change from the supine to standing position
- •History of pelvic radiotherapy
- •Pulmonary venous occlusive disease
研究者
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A prospective, randomized, double-blind, double-dummy, placebo- and active controlled, multicenter study assessing the efficacy and safety of the combination BAY 60 4552 / vardenafil compared to vardenafil (20 mg) for the treatment of erectile dysfunction not sufficiently responsive to standard therapy with PDE5 inhibitors - NDEUCTR2010-020122-18-ITBayer HealthCare AG267
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A prospective, randomized, double-blind, double-dummy, placebo- and active controlled, multicenter study assessing the efficacy and safety of the combination BAY 60 4552 / vardenafil compared to vardenafil (20 mg) for the treatment of erectile dysfunction not sufficiently responsive to standard therapy with PDE5 inhibitorsEUCTR2010-020122-18-SEBayer HealthCare AG267
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A prospective, randomized, double-blind, double-dummy, placebo- and active controlled, multicenter study assessing the efficacy and safety of the combination BAY 60 4552 / vardenafil compared to vardenafil (20 mg) for the treatment of erectile dysfunction not sufficiently responsive to standard therapy with PDE5 inhibitorsEUCTR2010-020122-18-NLBayer HealthCare AG
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A prospective, randomized, double-blind, double-dummy, placebo- and active controlled, multicenter study assessing the efficacy and safety of the combination BAY 60 4552 / vardenafil compared to vardenafil (20 mg) for the treatment of erectile dysfunction not sufficiently responsive to standard therapy with PDE5 inhibitorsErectile dysfunctionMedDRA version: 12.1Level: LLTClassification code 10061461Term: Erectile dysfunctionEUCTR2010-020122-18-FRBayer HealthCare AG
