- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Viagra AND sildenafil.
Displaying page 1 of 2.
EudraCT Number: 2011-004811-21 | Sponsor Protocol Number: s53584 | Start Date*: 2011-11-07 |
Sponsor Name:UZLeuven | ||
Full Title: The effect of Sildenafil citrate (Viagra ®) on stomach motility, gastric emptying and food intake in healthy volunteers | ||
Medical condition: study is conducted on healthy volunteers, no medical condition is investigated | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004171-37 | Sponsor Protocol Number: CH/2005/1944 | Start Date*: 2006-08-02 |
Sponsor Name:United Bristol Healthcare Trust | ||
Full Title: Oxidative Stress in children undergoing cardiopulmonary bypass: A trial of Sildenafil therapy | ||
Medical condition: Congenital Heart Disease | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003116-22 | Sponsor Protocol Number: RBK091 | Start Date*: 2006-12-21 |
Sponsor Name:Prof. Sechtem, Department of Cardiology, Robert Bosch Hospital | ||
Full Title: Application of Sildenafil in patients with documented coronary vasospasm in order to explore the pathophysiology of coronary vasospasm and the therapeutic effects of Sildenafil in patients sufferin... | ||
Medical condition: Coronary vasospasm is an abrupt severe vasoconstriction of coronary arteries leading to myocardial ischemia and angina pectoris. The reason for the occurrence of coronary spasm and the cellular mec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001034-32 | Sponsor Protocol Number: 05/CH/01 | Start Date*: 2006-02-02 |
Sponsor Name:NHS Greater Glasgow, Yorkhill | ||
Full Title: Does pre-operative Sildenafil protect against pulmonary related complications following cardiopulmonary bypass? A randomised trial in children undergoing cardiac surgical repair | ||
Medical condition: Congenital Heart Disease | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005333-39 | Sponsor Protocol Number: WS982821 | Start Date*: 2012-01-17 |
Sponsor Name:National and Kapodistrial University of Athens | ||
Full Title: The effects of acute sildenafil administration on inflammatory markers in patients with vasculogenic erectile dysfunction. | ||
Medical condition: vasculogenic erectile dysfunction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016096-29 | Sponsor Protocol Number: 08/0183 | Start Date*: 2010-03-05 |
Sponsor Name:University College London [...] | ||
Full Title: Pilot of oral Sildenafil for the treatment of Pulmonary Hypertension in Thalassaemia with comparison to controls. | ||
Medical condition: Pulmonary Hypertension in Thalassaemia patients | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001004-39 | Sponsor Protocol Number: JO-3 | Start Date*: 2005-07-05 |
Sponsor Name:University of Edinburgh | ||
Full Title: Investigation of combined phosphodiesterase 5 inhibitor and isosorbide mononitrate for the treatment of resistant hypertension | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
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 |
EudraCT Number: 2010-022996-79 | Sponsor Protocol Number: URO 2010 | Start Date*: 2010-12-31 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: On demand versus daily sildenafil for patients undergoing bilateral nerve sparing radical prostatectomy: a randomized, open label, parallel group trial. | |||||||||||||
Medical condition: radical prostatectomy | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001632-64 | Sponsor Protocol Number: CLCZ696B2225 | Start Date*: 2012-08-08 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open label, three-period, single sequence study to evaluate the pharmacokinetic drug-drug interaction between LCZ696 and sildenafil in subjects with mild to moderate hypertension | |||||||||||||
Medical condition: mild to moderate hypertension | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001591-30 | Sponsor Protocol Number: S-20150201 | Start Date*: 2017-11-06 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Treatment of congenital nephrogenic diabetes insipidus with a guanylate cyclase stimulator, riociguat or a phosphodiesterase type 5 inhibitor, sildenafil | |||||||||||||
Medical condition: Nephrogenic diabetes insipidus because of AVP2R-mutation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005139-61 | Sponsor Protocol Number: EB064 | Start Date*: 2006-10-24 |
Sponsor Name:Emotional Brain | ||
Full Title: Neural correlates of sexual arousal during treatment of testosterone combined with sildenafil in healthy female subjects with FSD. Effects of differing levels of attentional engagement on neural co... | ||
Medical condition: Hypoactive sexual desire disorder and female sexual arousal disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002688-28 | Sponsor Protocol Number: 66/2007/U/Sper | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Pilot study on the short-term effects of Sildenafil on hemodynamic response to exercise and exercise capacity in Fontan patients | |||||||||||||
Medical condition: congenital heart disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000021-57 | Sponsor Protocol Number: 01000 | Start Date*: 2006-03-10 |
Sponsor Name:Rigshospitalet | ||
Full Title: Bosentan and Sildenfil for patients with Eisenmenger syndrome | ||
Medical condition: Eisenmengers syndrome is condition with severe pulmonary arterial hypertension due to a shunting of blood from the left side of the heart to the right side of the heart. When the pressure in the pu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003971-19 | Sponsor Protocol Number: RP-01 | Start Date*: 2006-01-24 | |||||||||||
Sponsor Name:MEDA AB [...] | |||||||||||||
Full Title: Clinical study to evaluate the ability of MUSE to increase erectile function in post-radical prostatectomy patients - Randomised, controlled, open study with two parallel groups comparing MUSE 250... | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004112-63 | Sponsor Protocol Number: DutchSTRIDER | Start Date*: 2014-08-13 |
Sponsor Name:Academic Medical Center | ||
Full Title: The Dutch STRIDER (Sildenafil TheRapy In Dismal prognosis Early-onset intrauterine growth Restriction) Trial | ||
Medical condition: Fetal growth restriction | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
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: 2007-002009-31 | Sponsor Protocol Number: EB069 | Start Date*: 2007-06-13 |
Sponsor Name:Emotional Brain BV | ||
Full Title: A double blind randomized placebo controlled cross-over study to validate the distinction between women with different levels of attention and valence direction for erotic stimuli, in relation with... | ||
Medical condition: Hypoactive sexual desire disorder and female sexual arousal disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002411-25 | Sponsor Protocol Number: A1481237 | Start Date*: 2005-08-30 | |||||||||||
Sponsor Name:Pfizer Global Pharamceuticals, EuCAn, Pfizer Inc | |||||||||||||
Full Title: A prospective multicenter, parallel group study with a single blind phase and a double blind randomised phase, to evaluate the efficacy and satisfaction of Viagra® (Sildenafil Citrate) high dose (1... | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004167-20 | Sponsor Protocol Number: A1481252 | Start Date*: 2015-03-24 | ||||||||||||||||||||||||||
Sponsor Name:Pfizer Japan Inc | ||||||||||||||||||||||||||||
Full Title: A Phase 3, Multi-Center, Open-Label Study To Confirm Safety, Efficacy And Tolerability Of Sildenafil Citrate 20 Mg Three Times a Day (TID) In Subjects With Pulmonary Arterial Hypertension | ||||||||||||||||||||||||||||
Medical condition: Pulmonary Arterial Hypertension | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
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