- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Ejaculation.
Displaying page 1 of 2.
EudraCT Number: 2007-003171-39 | Sponsor Protocol Number: PSD502-PE-004 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Plethora Solutions Ltd | |||||||||||||
Full Title: A phase III, multi-centre, randomized, double-blind, placebo-controlled study, with open-label follow on, to evaluate the efficacy, safety and tolerability of PDS502 in subjects with Premature Ejac... | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011855-40 | Sponsor Protocol Number: OTB109059 | Start Date*: 2009-11-26 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Phase II Study to Evaluate: Delay in Intravaginal Ejaculatory Latency Time (IELT), Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two Oral Doses of GSK557296 in a Randomized, Doub... | |||||||||||||
Medical condition: Premature ejaculation. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011309-18 | Sponsor Protocol Number: R096769PRE4001 | Start Date*: 2009-12-02 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Prospective, Observational Study of Men With Premature Ejaculation Who Are Treated With PRILIGY™ or Alternate Care | |||||||||||||
Medical condition: premature ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001650-94 | Sponsor Protocol Number: 191622-133 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: An Exploratory Study of the Safety and Efficacy of BOTOX® for the Treatment of Premature Ejaculation | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000244-24 | Sponsor Protocol Number: A3871027 | Start Date*: 2004-08-18 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: A Phase 2b, multi-center, double-blind, placebo-controlled, parallel group dose response study to assess the efficacy and safety of oral UK-390,957 in men with premature ejaculation. | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) IT (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003650-15 | Sponsor Protocol Number: PSD502-PE-005 | Start Date*: 2008-12-29 | |||||||||||
Sponsor Name:Plethora Solutions Ltd | |||||||||||||
Full Title: A Phase II, multi-centre, double-blind, randomised, placebo-controlled, 4-way cross-over, dose-range finding study to evaluate efficacy and safety and tolerability of PSD502 in subjects with premat... | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005319-16 | Sponsor Protocol Number: SPE111155 | Start Date*: 2008-11-14 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: ``A double blind, parallel group, placebo controlled study to evaluate the effect of a single oral dose of GSK958108 on ejaculatory latency time (ELT) in male patients suffering from premature ejac... | |||||||||||||
Medical condition: Premature ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011411-21 | Sponsor Protocol Number: BVF-324-302 | Start Date*: 2009-07-17 | |||||||||||
Sponsor Name:Biovail Laboratories International SRL, c/o Biovail Technologies Ltd | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy and Safety of Two Doses of Tramadol Hydrochloride Orally Disintegrating Tablets in Male Subjects with Pre... | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: HU (Prematurely Ended) BG (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011410-18 | Sponsor Protocol Number: BVF-324-301 | Start Date*: 2009-07-29 | |||||||||||
Sponsor Name:Biovail Laboratories International SRL, c/o Biovail Technologies Ltd | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy and Safety of Two Doses of Tramadol Hydrochloride Orally Disintegrating Tablets in Male Subjects with Pre... | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) FR (Completed) SE (Prematurely Ended) ES (Completed) GB (Prematurely Ended) NL (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003737-13 | Sponsor Protocol Number: A3871028 | Start Date*: 2004-11-25 | |||||||||||
Sponsor Name:Pfizer Corporation Austria Ges.m.b.H., Clinical Research | |||||||||||||
Full Title: A Phase 2 multi-center, open label, long-term extension trial to assess the safety and sustained efficacy of oral UK-390,957 administered as required in adult men with premature ejaculation. | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) SE (Completed) CZ (Completed) GB (Prematurely Ended) DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004150-51 | Sponsor Protocol Number: A3871029 | Start Date*: 2004-12-10 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: A Phase 2 multi centre, double blind, placebo controlled flexible dose study to assess the efficacy and safety of oral UK-390,957 in men with premature ejaculation. | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013616-12 | Sponsor Protocol Number: R096769PRE3008 | Start Date*: 2010-04-12 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study of the Efficacy and Safety of Dapoxetine in Men With Premature Ejaculation and Concomitant Erectile Dy... | |||||||||||||
Medical condition: Premature ejaculation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002700-16 | Sponsor Protocol Number: R096769-PRE-3001 | Start Date*: 2004-12-14 |
Sponsor Name:Janssen-Cilag International N.V. | ||
Full Title: A Placebo-Controlled, Double-Blind, Randomized, Parallel-Group Study of the Efficacy and Safety of Dapoxetine in the Treatment of Subjects With Premature Ejaculation | ||
Medical condition: Premature Ejaculation (PE) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: CZ (Completed) FI (Completed) HU (Completed) GB (Completed) SE (Completed) DE (Completed) AT (Completed) ES (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-004065-42 | Sponsor Protocol Number: VR776/008 | Start Date*: 2006-01-23 |
Sponsor Name:Vectura Group plc | ||
Full Title: Phase II, double blind, intermittent dose, placebo controlled, randomised, two period crossover study to investigate the effect of inhaled doses of VR776 administered via Aspirair inhaler on IVELT ... | ||
Medical condition: Premature ejaculation | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004761-15 | Sponsor Protocol Number: 1 | Start Date*: 2005-10-12 |
Sponsor Name:City University | ||
Full Title: Rapid Ejaculation: An exploration of the pharmacological and behavioural therapies in men living in East London and a preliminary trial of these treatment modalities | ||
Medical condition: Premature ejaculation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011499-31 | Sponsor Protocol Number: SIA-001-2008 | Start Date*: 2009-08-05 | |||||||||||
Sponsor Name:SOCIETA` ITALIANA DI ANDROLOGIA | |||||||||||||
Full Title: STUDIO PROSPETTICO RANDOMIZZATO DI VALUTAZIONE DEI DIFFERENTI APPROCCI TERAPEUTICI AL DISAGIO SESSUALE AD ESPRESSIONE SULLA SFERA ERETTILE | |||||||||||||
Medical condition: DISAGIO SESSUALE: “Condizione e/o senso di inadeguatezza, non a carattere transitorio, tale da provocare una compromissione della salute sessuale (OMS working definition). L’inadeguatezza puo' orig... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010549-30 | Sponsor Protocol Number: 44/09 | Start Date*: 2009-12-16 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PRAMIPEXOLE IN THE MALE LIBIDO FAILURE : A PHASE II, off-label, pilot study | |||||||||||||
Medical condition: male libido failure | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001511-70 | Sponsor Protocol Number: 44313 | Start Date*: 2015-08-05 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Efficacy, safety and tolerability of lacosamide in patients with gain-of-function Nav1.7 mutations related small fiber neuropathy: a randomized, double-blind, placebo controlled, crossover trial | ||
Medical condition: SCN9A mutation related small fiber neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002897-27 | Sponsor Protocol Number: 18E-Prg06 | Start Date*: 2018-12-21 | |||||||||||
Sponsor Name:IBSA, Institut Biochimique, S.A. | |||||||||||||
Full Title: A proof of concept, randomized, controlled clinical trial to assess the efficacy of subcutaneous progesterone (Prolutex) versus vaginal proges-terone (Progeffik) for endometrial preparation in wome... | |||||||||||||
Medical condition: Infertility. Assisted Reproductive Tecniques. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004784-20 | Sponsor Protocol Number: BER-PRO-2014-01 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Instituto Bernabeu | |||||||||||||
Full Title: Subcutaneous progesterone ( Prolutex ) versus vaginal progesterone capsules (Progeffik) for endometrial preparation in fresh donated oocyte recipients: A prospective, randomized, single-blind, pi... | |||||||||||||
Medical condition: Infertility. Assisted Reproductive Techniques. Fresh donated oocyte recipients | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
