- Trials with a EudraCT protocol (196)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
196 result(s) found for: Sexual Dysfunction.
Displaying page 1 of 10.
EudraCT Number: 2006-004397-27 | Sponsor Protocol Number: 310741 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Bayer Schering Pharma AG | |||||||||||||
Full Title: Multi-center, double-blind, placebo-controlled study to investigate the efficacy and safety of daily oral 100 mg dehydroepiandrosterone (DHEA) over 6 treatment cycles as a concomitant therapy to or... | |||||||||||||
Medical condition: Multi-center, double-blind, placebo-controlled study to investigate the efficacy and safety of daily oral 100 mg dehydroepiandrosterone (DHEA) over 6 treatment cycles as a concomitant therapy to or... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001966-40 | Sponsor Protocol Number: CD001 | Start Date*: 2014-01-27 | ||||||||||||||||
Sponsor Name:Companion Diagnostics BV | ||||||||||||||||||
Full Title: A double blind, randomized, placebo controlled, cross-over, Lybridos dose finding study to validate the predictive power of the diagnostic model for Lybrido and Lybridos efficacy and to identify an... | ||||||||||||||||||
Medical condition: Hypoactive Sexual Desire Disorder/SSRI-induced sexual dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000013-10 | Sponsor Protocol Number: PR3042 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:Pantarhei Bioscience B.V. | |||||||||||||
Full Title: A double-blind, placebo controlled, randomised, comparative 2-way crossover study to determine the effect of concomitant treatment with dehydroepiandrosterone (50 mg) on sexual arousability and the... | |||||||||||||
Medical condition: Sexual dysfunction caused by the use of oral contraceptives | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007704-28 | Sponsor Protocol Number: EB77 | Start Date*: 2009-01-21 | |||||||||||
Sponsor Name:Emotional Brain | |||||||||||||
Full Title: Lybridos PoC: A double blind, randomized, cross-over placebo controlled pilot study to investigate the subjective and physiological efficacy and safety of Lybridos in healthy female subjects with F... | |||||||||||||
Medical condition: Female Sexual Dysfunction, specifically Hypoactive Sexual Desire Disorder, with or without Female Sexual Arousal Disorder. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002922-51 | Sponsor Protocol Number: H6D-MC-LVGH | Start Date*: 2006-10-16 | |||||||||||
Sponsor Name:Lilly ICOS LLC | |||||||||||||
Full Title: Tadalafil 5 mg Once a Day Compared to Placebo in Improving Erectile Dysfunction and Sexual Quality of Life | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001418-14 | Sponsor Protocol Number: VELOCE | Start Date*: 2019-07-11 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Assessment of clinical efficacy of Sildenafil 75 mg orodispersable film vs Sildenafil 100 mg tablet in patients with erectile dysfunction | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001033-41 | Sponsor Protocol Number: H6D-MC-LVFZ | Start Date*: 2004-09-22 | |||||||||||
Sponsor Name:ELI LILLY | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel-Design, Placebo-Controlled Study to Evluate the Efficacy and Safety of Tadalafil (2.5 mg e 5 mg) administered once daily to men with diabetes mellitus and erect... | |||||||||||||
Medical condition: Therapy of erectile disfunction to subjects with diabetes mellitus and erectile disfunction with a 2.5 mg or 5 mg daily dosing. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000580-10 | Sponsor Protocol Number: H6D-HL-LVGD | Start Date*: 2004-08-03 | |||||||||||
Sponsor Name:Oy Eli Lilly Finland Ab | |||||||||||||
Full Title: Effect of Tadalafil on the Quality of Life and Sexual Life Satisfaction in Erectile Dysfunction (ED) Patients Previously Treated with other Oral ED therapy | |||||||||||||
Medical condition: Erectile dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001549-13 | Sponsor Protocol Number: VAR102372 | Start Date*: 2004-09-14 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A pilot, randomized, double-blind, placebo-controlled, crossover study evaluating the efficacy and safety of Vardenafil versus placebo administered 12, 18 and 24 hours prior to initiation of sexual... | |||||||||||||
Medical condition: ERECTILE DISFUNCTION | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019540-39 | Sponsor Protocol Number: EB80 | Start Date*: 2010-05-12 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Emotional Brain | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A double blind, randomized, cross-over placebo controlled study to investigate the efficacy of sublingual testosterone solution on physiological and subjective arousal in healthy, sexually dysfunct... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: This pharmacodynamic trial will be conducted in sexually dysfunctional otherwise healthy women, but it is a part of a developmental program for medicine for Hypoactive Sexual Desire Disorder (comor... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019285-86 | Sponsor Protocol Number: EB79 | Start Date*: 2010-05-07 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Emotional Brain | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A single blind, randomized, cross-over placebo controlled dose finding study to investigate the pharmacokinetic profile of 3 doses of sublingual testosterone solution and their effect on physiologi... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: This pharmacokinetic trial will be conducted in healthy women, but it is a part of a developmental program for medicine for Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunct... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002770-23 | Sponsor Protocol Number: EB91 | Start Date*: 2011-07-04 | ||||||||||||||||||||||||||
Sponsor Name:Emotional Brain BV | ||||||||||||||||||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, proof of concept study to investigate the safety and efficacy of the combined administration of 0.5 mg sublingual testosterone and 10 mg tadalafil in... | ||||||||||||||||||||||||||||
Medical condition: Hypoactive Sexual Desire Disorder | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016790-15 | Sponsor Protocol Number: EB78 | Start Date*: 2009-12-03 |
Sponsor Name:Emotional Brain | ||
Full Title: A double blind, randomized, cross-over placebo controlled study to investigate the subjective and physiological efficacy and safety of Lybrido and Lybridos in the domestic setting in healthy female... | ||
Medical condition: Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunctions e.g Female Sexual Arousal Disorder (FSAD) is allowed) and/or SSRI induced sexual dysfunctioning. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000536-40 | Sponsor Protocol Number: BAY38-9456/12093 | Start Date*: 2008-03-29 | |||||||||||
Sponsor Name:Bayer HealthCare AG, D-51368 Leverkusen, Germany | |||||||||||||
Full Title: Pivotal phase III trial to investigate the efficacy and safety of an Orodispersible Tablet vardenafil versus placebo in the treatment of men with Erectile dysfunction (ED) - a fixed-dose, double-bl... | |||||||||||||
Medical condition: Erectile Dysfunction (ED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) DE (Completed) FR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001036-31 | Sponsor Protocol Number: A8361011 | Start Date*: 2007-06-25 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent. UK. CT13 9NJ | |||||||||||||
Full Title: A 2-COHORT, MULTI-CENTRE, RANDOMIZED, DOUBLE BLIND (3RD PARTY OPEN), PLACEBO CONTROLLED 4-WAY CROSSOVER STUDY TO ASSESS THE EFFICACY OF SINGLE ORAL DOSES OF PF-00446687 ON ERECTILE FUNCTION IN MEN ... | |||||||||||||
Medical condition: Male erectile dysfunction (MED). | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007670-38 | Sponsor Protocol Number: L00074-TD401 | Start Date*: 2008-06-23 | ||||||||||||||||
Sponsor Name:Pierre Fabre Médicament | ||||||||||||||||||
Full Title: "Evaluation of erectyle disfonction in patients suffering from testosterone deficiency, before and after tretament by Testopatch" | ||||||||||||||||||
Medical condition: Testosterone deficiency Erectile dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001579-32 | Sponsor Protocol Number: RHF0001 | Start Date*: 2008-09-22 | |||||||||||
Sponsor Name:University of Hertfordshire | |||||||||||||
Full Title: Erectile dysfunction:a randomised controlled trial of lipid lowering with simvastatin (EDS trial) | |||||||||||||
Medical condition: Erectile dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003290-25 | Sponsor Protocol Number: A1481239 | Start Date*: 2005-12-23 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: A multicenter, double-blind placebo controlled, fixed dose study with an open-label, flexible dose phase to assess the efficacy of Sildenafil Citrate in providing a better sexual experience includi... | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002735-32 | Sponsor Protocol Number: EB72 | Start Date*: 2008-06-24 |
Sponsor Name:Emotional Brain | ||
Full Title: A double blind, randomized, placebo controlled cross-over study to investigate the subjective and physiological efficacy and safety of Lybrido and Lybridos in the domestic setting in healthy female... | ||
Medical condition: Hypoactive sexual desire disorder and female sexual arousal disorder in combination with SSRI use. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-000360-45 | Sponsor Protocol Number: A1481222 | Start Date*: 2005-05-12 | |||||||||||
Sponsor Name:PFIZER | |||||||||||||
Full Title: A MULTICENTER, PARALLEL GROUP FLEXIBLE DOSE STUDY WITH A DOUBLE BLIND, RANDOMIZED, PLACEBO CONTROLLED PHASE AND AN OPEN-LABEL PHASE TO EVALUATE THE QUALITY OF ERECTIONS IN MEN WITH ERECTILE DYSFU... | |||||||||||||
Medical condition: Erectil Dysfunction | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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