- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Energy Drinks.
Displaying page 1 of 1.
EudraCT Number: 2021-002909-10 | Sponsor Protocol Number: P137 | Start Date*: 2022-10-24 |
Sponsor Name:Maastricht University | ||
Full Title: THE IMPACT OF PSILOCYBIN ON PAIN IN FIBROMYALGIA PATIENTS AND HEALTHY VOLUNTEERS: A MULTICENTER TRIAL | ||
Medical condition: Fibromyalgia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002142-38 | Sponsor Protocol Number: 292008 | Start Date*: 2009-02-16 |
Sponsor Name:NV Organon | ||
Full Title: A phase I, single center, open-label parallel group trial to compare the pharmacokinetics of NOMAC between healthy female adolescents (aged 14-17 years) and healthy female adults (aged 18-50 years)... | ||
Medical condition: Hormonal oral contraception in healthy women | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004412-22 | Sponsor Protocol Number: U-2013-007 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:UCR Uppsala Clinical Research Center | |||||||||||||
Full Title: TRIAL OF CAFFEINE TO ALLEVIATE DYSPNEA RELATED TO TICAGRELOR (TROCADERO) A double-blinded, placebo-controlled, randomized, multicenter, development phase II study | |||||||||||||
Medical condition: Dyspnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005256-33 | Sponsor Protocol Number: 1182.107 | Start Date*: 2007-09-14 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | |||||||||||||
Full Title: Ensayo clínico multicéntrico, aleatorizado y abierto para evaluar tres dosis de Tipranavir potenciado con dosis bajas de ritonavir (500mg/200mg una vez al día, 250mg/100 mg dos veces al día y 500 m... | |||||||||||||
Medical condition: Los pacientes de este estudio deben ser varones y mujeres con edades comprendidas entre los 18 y los 65 años de edad infectados por VIH-1 y no tratados anteriormente con antirretrovirales. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004009-37 | Sponsor Protocol Number: MD2021.01 | Start Date*: 2021-11-05 | ||||||||||||||||
Sponsor Name:Prothya Biosolutions BV | ||||||||||||||||||
Full Title: A Phase 1/2 study of the dose-response in pharmacodynamics and safety of prothrombin complex concentrate Cofact in healthy subjects under vitamin K antagonist anticoagulation | ||||||||||||||||||
Medical condition: Treatment of bleeding and perioperative prophylaxis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004342-28 | Sponsor Protocol Number: PKFT218-1602 | Start Date*: 2017-10-30 | |||||||||||
Sponsor Name:Flamel Ireland Ltd trading under the business name Avadel Ireland | |||||||||||||
Full Title: A comparative, open label, randomized, 2 periods, 2 sequence crossover study to assess the relative bioavailability of sodium oxybate for extended release oral suspension (FT218) formulation (singl... | |||||||||||||
Medical condition: A trial on healthy volunteer fore the development of a treatment for cataplexy and excessive daytime sleepiness in narcolepsy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
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