- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Potassium nitrate.
Displaying page 1 of 1.
EudraCT Number: 2009-016655-21 | Sponsor Protocol Number: P-090756-01 | Start Date*: 2010-04-30 | |||||||||||
Sponsor Name:Ferrer Internacional, S.A | |||||||||||||
Full Title: A Multi-Centre, Randomized, Placebo-controlled, Parallel-Group, Double-Blinded Study to Compare the Therapeutic Efficacy, Safety and Tolerability of 3 Single Vaginal Doses of Arasertaconazole Nitra... | |||||||||||||
Medical condition: Vulvovaginal Candidiasis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) FR (Completed) LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003407-17 | Sponsor Protocol Number: CLD-1-2021 | Start Date*: 2022-04-19 | |||||||||||
Sponsor Name:University Clinic of Nephrology and Hypertension | |||||||||||||
Full Title: Combined effects of potassium, nitrate and sodium on blood pressure in patients with hypertension | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001636-60 | Sponsor Protocol Number: SL-3-2019 | Start Date*: 2019-07-12 | |||||||||||
Sponsor Name:University clinic of Nephrology and Hypertension, Regional Hospital Holstebro | |||||||||||||
Full Title: The effect of spironolactone on renal hemodynamics in patients with essential hypertension | |||||||||||||
Medical condition: Physiological responses in patients with essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002910-12 | Sponsor Protocol Number: 0017 | Start Date*: 2005-06-17 | |||||||||||
Sponsor Name:Theravance Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Vancomycin for Treatment of Complicated Gram-Positive Skin and Skin Structure Infections with a focus on Pa... | |||||||||||||
Medical condition: Complicated Gram-Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-Resistant Staphylococcus aureus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005992-81 | Sponsor Protocol Number: CL-N-CSM-III/01/08 | Start Date*: 2011-03-21 | |||||||||||
Sponsor Name:Dr. F. Köhler Chemie GmbH | |||||||||||||
Full Title: A Prospective Randomized Double Blind Multicenter Phase III Study Comparing two Methods of Cardioplegia in Coronary Artery Bypass Surgery Custodiol-N versus Custodiol | |||||||||||||
Medical condition: The study population will be selected from both genders with coronary artery disease (CAD) who are to undergo cardiopulmonary bypass for coronary artery bypass surgery. The ratio of incidence for b... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002914-12 | Sponsor Protocol Number: 0018 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:Theravance Inc. | |||||||||||||
Full Title: A phase 3, Randomized, Double-Blind, Multinational Trial of Intravenous Televancin Versus Vancomycin for Treatment of Complicated Gram-positive Skin and Skin Structure Infections with a focus on Pa... | |||||||||||||
Medical condition: Complicated Gram-Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-Resistant Staphylococcus aureus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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