- Trials with a EudraCT protocol (46)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
46 result(s) found for: potasio.
Displaying page 1 of 3.
EudraCT Number: 2008-002191-98 | Sponsor Protocol Number: PREVARENAL-08 | Start Date*: 2008-11-27 |
Sponsor Name:Servicio de Nefrologia-Hospital Universitario Vall d'Hebron | ||
Full Title: "Efecto del ARA-II Olmesartan sobre el metabolismo del potasio en pacientes con insuficiencia renal crónica" | ||
Medical condition: Microalbuminúria, hipertensión arterial y renoprotección en la insuficiencia renal crónica. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014313-27 | Sponsor Protocol Number: RAL-IC | Start Date*: 2009-11-11 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: ESTUDIO PILOTO PARA COMPARAR LOS PARÁMETROS FARMACOCINÉTICOS EN PLASMA E INTRACELULARES DE RALTEGRAVIR ADMINISTRADO UNA VEZ AL DÍA EN PACIENTES ADULTOS INFECTADOS POR EL VIH. | |||||||||||||
Medical condition: Infección VIH-1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004460-66 | Sponsor Protocol Number: KARAASS-1 | Start Date*: 2014-04-01 | ||||||||||||||||
Sponsor Name:Jørgen Jeppesen | ||||||||||||||||||
Full Title: Oral potassium supplementation in healthy men - interactions with the renin-angiotensin-aldosterone system and the sympathetic nervous system | ||||||||||||||||||
Medical condition: Blood pressure regulation and hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-014480-39 | Sponsor Protocol Number: LLC-RAET-2009-1 | Start Date*: 2010-02-18 |
Sponsor Name:Luis Fernando López Cortés | ||
Full Title: Concentraciones plasmáticas e intracelulares de Raltegravir y Etravirina administrados una vez al día (800 mg y 400 mg, respectivamente) comparado con su dosificación estándard (400 mg y 200 mg/12 ... | ||
Medical condition: Pacientes con infección por el VIH en tratamiento con raltegravir o etravirina. HIV-Patients on treatment with raltegravir or etravirine | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005473-35 | Sponsor Protocol Number: DISCOR-RAL | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: PILOT STUDY TO ASSESS THE ROLE OF IMMUNE ACTIVATION AND APOPTOSIS AS A MARKER FOR TREATMENT INTENSIFICATION WITH RALTEGRAVIR IN HIV-INFECTED PATIENTS ON ANTIRETROVIRAL THERAPY WITH LONG-TERM VIRAL ... | |||||||||||||
Medical condition: Infección VIH-1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005663-34 | Sponsor Protocol Number: EC20081 | Start Date*: 2009-06-26 |
Sponsor Name:Joseba Andoni Santamaría Zuazua | ||
Full Title: Ensayo clínico sobre la eficacia de una pauta con amoxicilina/clavulánico 2000/125 mg (GE) cada doce horas, frente a placebo(GC) en la prevención de la infeccion postoperatoria tras la exodoncia de... | ||
Medical condition: prevención de la infección postoperatorioa tras la exodoncia de terceros molares totalmente incluidos recubiertos por hueso mandibular | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019135-35 | Sponsor Protocol Number: PillCam2010 | Start Date*: 2010-06-11 | |||||||||||
Sponsor Name:Dr. Enrique | |||||||||||||
Full Title: Evaluación de la limpieza intestinal en un día para la colonoscopia con cápsula colónica: estudio piloto | |||||||||||||
Medical condition: Detección de Cancer colorrectal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021360-15 | Sponsor Protocol Number: IG0905 | Start Date*: 2010-12-20 | |||||||||||
Sponsor Name:Instituto Grifols S.A. | |||||||||||||
Full Title: "EFECTOS DEL RECAMBIO PLASMÁTICO SOBRE LA CAPACIDAD FUNCIONAL DE LA ALBÚMINA SÉRICA, LA DISFUNCIÓN CIRCULATORIA, LA FUNCION RENAL Y CEREBRAL EN PACIENTES CIRRÓTICOS CON ACUTE-ON-CHRONIC LIVER FAIL... | |||||||||||||
Medical condition: Pacientes cirróticos con "Acute on chronic liver failure" | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022901-16 | Sponsor Protocol Number: TRAMA | Start Date*: 2011-07-28 | ||||||||||||||||
Sponsor Name:Gemma Rialp | ||||||||||||||||||
Full Title: Estudio multicéntrico sobre el efecto del tratamiento de la alcalosis metabólica con acetazolamida en la duración de la ventilación mecánica. | ||||||||||||||||||
Medical condition: Enfermedad pulmonar obstructiva crónica y síndrome de obesidad ventilación | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001270-77 | Sponsor Protocol Number: TRASVAL | Start Date*: 2005-03-01 |
Sponsor Name:Equipo de doctores: Dr. Amado Andrés y Dr. Manuel Praga | ||
Full Title: Estudio piloto para evaluar la eficacia y seguridad de Valsartán para el control de la progresión de la insuficiencia renal y la morbimortalidad cardiovascular en pacientes con trasplante renal fun... | ||
Medical condition: Pacientes varones y mujeres de 18 a 70 años con trasplantes renales funcionantes de más de 1 año de evolución y una insuficiencia renal leve o moderada (creatinina sérica > 1,3 mg/dl en mujeres y >... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001192-29 | Sponsor Protocol Number: cv-08/025 | Start Date*: 2008-06-03 |
Sponsor Name:Fundación Investigación y Desarrollo en el Area Cardiovascular | ||
Full Title: “Evaluación mediante proteómica de biomarcadores proteicos asociados con el tratamiento con Eplerenona versus espironolactona en pacientes post-infarto agudo de miocardio, diabéticos con hipertensi... | ||
Medical condition: Disfunción ventricular leve-moderada post-infarto agudo de miocardio en pacientes diabéticos con hipertensión arterial no controlada. Low-moderate ventricular dysfunction in post-acute coronary sy... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007044-10 | Sponsor Protocol Number: EC07/90842 | Start Date*: 2008-03-04 |
Sponsor Name:JOSÉ ANTONIO SERRANO TRENAS | ||
Full Title: UTILIDAD DEL HIERO INTRAVENOSO EN EL PACIENTE ANCIANO CON FRACTURA DE CADERA | ||
Medical condition: SE INVESTIGA LA POSIBILIDAD DE REDUCCIÓN DE LAS NECESIDADES TRANSFUSIONALES DE LOS PACIENTES ANCIANOS INTERVENIDOS DE FRACTURA DE CADERA MEDIANTE SU TRATAMIENTO CON HIERRO INTRAVENOSO. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012963-33 | Sponsor Protocol Number: CORTEEC | Start Date*: 2010-10-04 | |||||||||||
Sponsor Name:ALFREDO TAGARRO GARCIA | |||||||||||||
Full Title: ENSAYO CLINICO FASE II CORTICOIDES PARA EL EMPIEMA Y EL DERRAME PLEURAL PARANEUMÓNICO EN NIÑOS MULTICENTRIC, PHASE II, CLINICAL TRIAL CORTICOIDS FOR EMPYEMA AND PLEURAL EFFUSION IN CHILDREN | |||||||||||||
Medical condition: DERRAME PLEURAL PARANEUMONICO (PARAPNEUMONIC PLEURAL EFFUSSION) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-005030-38 | Sponsor Protocol Number: PAT-CR-302 | Start Date*: 2019-08-10 | |||||||||||
Sponsor Name:Vifor Pharma, Inc. | |||||||||||||
Full Title: A Multicenter, Double-blind, Placebo-controlled, Randomized Withdrawal, Parallel Group Study of Patiromer for the Management of Hyperkalemia in Subjects Receiving Renin-Angiotensin-Aldosterone Syst... | |||||||||||||
Medical condition: Management of hyperkalemia due to renin-angiotension-aldosterone system medications in patients treated for heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) CZ (Completed) NL (Completed) ES (Ongoing) HU (Completed) DE (Completed) BG (Completed) GB (GB - no longer in EU/EEA) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014406-34 | Sponsor Protocol Number: ORVACS-010 | Start Date*: 2010-05-28 | |||||||||||
Sponsor Name:ORVACS | |||||||||||||
Full Title: International, multicenter, randomized, non-comparative controlled study of therapeutic intensification plus immunomodulation in HIV patients with long-term viral suppression | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) GB (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005468-28 | Sponsor Protocol Number: CQAB149B2340 | Start Date*: 2008-01-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase III, randomized, double-blind, placebo controlled, multicenter, 3-period, 14 day crossover study to determine the 24-h lung function profile of indacaterol (300 μg o.d.) in patients with mo... | |||||||||||||
Medical condition: moderate to severe chronic obstructive pulmonary disease (COPD). | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013093-41 | Sponsor Protocol Number: AC220-002 | Start Date*: 2010-02-05 | |||||||||||
Sponsor Name:Ambit Biosciences Corporation | |||||||||||||
Full Title: A PHASE 2 OPEN-LABEL, AC220 MONOTHERAPY EFFICACY (ACE) STUDY IN PATIENTS WITH ACUTE MYELOID LEUKEMIA (AML) WITH FLT3-ITD ACTIVATING MUTATIONS | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) NL (Completed) PL (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017950-11 | Sponsor Protocol Number: ING113086 | Start Date*: 2010-11-10 | |||||||||||
Sponsor Name:ViiV Healthcare S.L | |||||||||||||
Full Title: Estudio fase III, aleatorizado, doble ciego, para evaluar la eficacia y la seguridad de 50 mg de GSK1349572 una vez al día, frente a 400mg de raltegravir dos veces al día, ambos administrados con u... | |||||||||||||
Medical condition: Pacientes adultos infectados por el VIH-1 que no han recibido tratamiento antirretroviral previo | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) FR (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012616-40 | Sponsor Protocol Number: CAMN107A2405 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An Open Label, Randomized Study of Nilotinib vs. Standard Imatinib (400/600 mg QD) Comparing the Kinetics of Complete Molecular Response for CML-CP Patients with Evidence of Persistent Leukemia by ... | |||||||||||||
Medical condition: Chronic Myelogenous Leukemia in Chronic Phase | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010208-27 | Sponsor Protocol Number: CLCZ696B2214 | Start Date*: 2009-06-29 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A | |||||||||||||
Full Title: Estudio aleatorizado, doble ciego, multicéntrico, de grupos paralelos, controlado con tratamiento activo de doce semanas de seguimiento para evaluar la eficacia, seguridad y tolerabilidad de LCZ696... | |||||||||||||
Medical condition: Insuficiencia Cardiaca crónica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) IT (Completed) PL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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