- Trials with a EudraCT protocol (719)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
719 result(s) found for: Body temperature.
Displaying page 1 of 36.
EudraCT Number: 2007-006232-58 | Sponsor Protocol Number: UFC-08/01 | Start Date*: 2008-01-31 | ||||||||||||||||
Sponsor Name:Hospital general Universitario de Alicante | ||||||||||||||||||
Full Title: Ensayo clínico aleatorizado y controlado con paracetamol de la seguridad renal de metamizol en el tratamiento de pacientes cirróticos con y sin ascitis (Randomized Controlled Clinical Trial to stu... | ||||||||||||||||||
Medical condition: Dolor y/o fiebre en pacientes cirróticos con o sin descompensación ascítica | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002449-36 | Sponsor Protocol Number: ALGINF-2006/01 | Start Date*: 2006-10-23 | |||||||||||
Sponsor Name:Laboratorio de Aplicaciones Farmacodinámicas S.A. | |||||||||||||
Full Title: Ensayo clínico, multicéntrico, aleatorizado, simple ciego, paralelo, para evaluar la eficacia antipirética de lisinato de ibuprofeno versus ibuprofeno base en niños con procesos febriles. Multicent... | |||||||||||||
Medical condition: Procesos febriles en población infantil. Febrile processes in child population. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003362-27 | Sponsor Protocol Number: WO17.123 | Start Date*: 2018-03-02 |
Sponsor Name:OLVG | ||
Full Title: Ketanserin effects on Peripheral Temperature and Lactate | ||
Medical condition: Critical illness Delta temperature greater than 6.0 °C | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002548-18 | Sponsor Protocol Number: Studie1hemodynami | Start Date*: 2016-10-04 |
Sponsor Name:Karolinska Institutet Södersjukhuset | ||
Full Title: Hemodynamic effects from administration of body temperature warmed versus room temperature fluid boluses in healthy volunteers | ||
Medical condition: This trial will be a crossover study of healthy volunteers receiving a warm vs a cold fluid bolus to investigate the difference in hemodynamic response. While this will generate data for future stu... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002512-27 | Sponsor Protocol Number: NL44774.068.13 | Start Date*: 2013-11-25 |
Sponsor Name:Maastricht University | ||
Full Title: The role of bile acids in human brown adipose tissue metabolism | ||
Medical condition: Healthy subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021437-30 | Sponsor Protocol Number: PAISII-V01 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:ErasmusMC | |||||||||||||
Full Title: Paracetamol (Acetaminophen) in Stroke 2 (PAIS 2): A randomized, placebo-controlled clinical trial of high-dose paracetamol in patients with acute stroke and a body temperature of 36.5°C or above | |||||||||||||
Medical condition: acute stroke (cerebral infarction or intracrebral hemorrhage) and a body temperature of 36.5 degrees or above. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002119-16 | Sponsor Protocol Number: NORM2016-IQ | Start Date*: 2016-11-10 | |||||||||||
Sponsor Name:Aflofarm Farmacja Polska Sp. z o.o. | |||||||||||||
Full Title: Multi-center phase 3 clinical study of fever reduction effectiveness in children age 24-72 months using combined therapy (ibuprofen plus paracetamol) compared to monotherapy with paracetamol and/or... | |||||||||||||
Medical condition: Fever due to viral infection | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005128-12 | Sponsor Protocol Number: T705-COVID-GCRI-Protocol-A | Start Date*: 2021-02-01 |
Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
Full Title: An Investigation of the Efficacy and Safety of Favipiravir in COVID-19 Patients with Mild Pneumonia − An open-label randomized controlled study | ||
Medical condition: COVID-19 Patients with Mild Pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Prohibited by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019830-29 | Sponsor Protocol Number: 3621 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Hopitaux Universitaires de Strasbourg | |||||||||||||
Full Title: Evaluation of the effects of CO2 insufflation on central body temperature and on postoperative pain in laparoscopic surgery | |||||||||||||
Medical condition: Elective videolaparoscopic hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002955-20 | Sponsor Protocol Number: ADENO-beta | Start Date*: 2023-11-22 | |||||||||||
Sponsor Name:AOU CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO | |||||||||||||
Full Title: Double-blind randomized controlled study versus placebo to evaluate the efficacy of mono-administration of betamethasone in children with symptomatic Adenovirus infection (ADENO-beta). | |||||||||||||
Medical condition: Pediatric patients diagnosed with symptomatic Adenovirus infection. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005079-17 | Sponsor Protocol Number: 06-IN-AK004 | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:Nektar Therapeutics | |||||||||||||
Full Title: An Open-Label, Multicenter, Multinational Study to Assess the Safety, Tolerability and Pharmacokinetics of Aerosolized Amikacin in Intubated and Mechanically-Ventilated Patients with Nosocomial Pne... | |||||||||||||
Medical condition: Nosocomial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001733-86 | Sponsor Protocol Number: 1710 | Start Date*: 2014-10-15 |
Sponsor Name:Maastricht University | ||
Full Title: The effect of L-arginine on brown adipose tissue metabolism in South Asian and white Caucasian subjects | ||
Medical condition: Obesity, glucose intolerance, endothelial dysfunction | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001760-29 | Sponsor Protocol Number: ALCOVID-19 | Start Date*: 2020-09-09 |
Sponsor Name:Sociedad Española de Farmacia Hospitalaria | ||
Full Title: Phase II clinical trial to evaluate the efficacy and safety of inhaled ethanol in the treatment of early-stage COVID-19. | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005510-20 | Sponsor Protocol Number: C10953/1100 | Start Date*: 2013-03-07 |
Sponsor Name:Cephalon, Inc. | ||
Full Title: A Randomized, Open-Label Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Single and Multiple Doses of Armodafinil (50, 100, and 150 mg/day) in Children and Adolescents w... | ||
Medical condition: Excessive Sleepiness associated with Narcolepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-001117-42 | Sponsor Protocol Number: DORI-NOS-2001 | Start Date*: 2007-10-18 | ||||||||||||||||
Sponsor Name:Janssen Cilag International NV | ||||||||||||||||||
Full Title: A Randomized, Open-Label, Multicenter Study to Assess the Safety and Tolerability of Doripenem Compared With Imipenem in the Treatment of Subjects With Complicated Intra-Abdominal Infections or Ven... | ||||||||||||||||||
Medical condition: ventilator-associated pneumonia complicated intra-abdominal infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001026-22 | Sponsor Protocol Number: 1813T0835 | Start Date*: 2021-03-05 |
Sponsor Name:Shionogi & Co., Ltd. | ||
Full Title: An Open-label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Baloxavir Marboxil 2% Granules after Administration of a Single Dose to Otherwise Healthy Pediatric Patient... | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-003561-16 | Sponsor Protocol Number: TAK-242/01-04-TL-242-011 | Start Date*: 2005-12-21 | |||||||||||
Sponsor Name:Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: A Pivotal, Multicentre, Multinational, Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TAK-242 in Adults with Severe Sepsis | |||||||||||||
Medical condition: Severe sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) FI (Prematurely Ended) AT (Prematurely Ended) CZ (Prematurely Ended) SE (Prematurely Ended) ES (Completed) PT (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001730-17 | Sponsor Protocol Number: BAP00248/307 | Start Date*: 2004-09-16 | |||||||||||
Sponsor Name:Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | |||||||||||||
Full Title: A Phase 3, Randomized Double-Blind Study of Ceftobiprole Medocaril Versus Linezolid Plus Ceftazidime in the Treatment of Nosocomial Pneumonia | |||||||||||||
Medical condition: Nosocomial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) HU (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005214-18 | Sponsor Protocol Number: T705-COVID-GCRI-Protocol-B | Start Date*: 2021-02-01 |
Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
Full Title: An Investigation of the Efficacy and Safety of Favipiravir in COVID-19 Patients without Pneumonia − An open-label randomized controlled study | ||
Medical condition: COVID-19 Patients without Pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Prohibited by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005466-19 | Sponsor Protocol Number: R0002198 | Start Date*: 2014-05-26 |
Sponsor Name:RadboudUMC | ||
Full Title: Cytokine inhibition in Chronic Fatigue Syndrome patients - a pilot study. | ||
Medical condition: Chronic Fatigue Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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