- Trials with a EudraCT protocol (2,192)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,192 result(s) found for: End of life care.
Displaying page 1 of 110.
EudraCT Number: 2017-000039-16 | Sponsor Protocol Number: LUMC-PHEG-20172022 | Start Date*: 2017-10-10 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Paracetamol to enhance quality of life and daily function and to decrease care dependency in advanced dementia: A randomized, double-blind, placebo-controlled crossover trial in long-term care faci... | |||||||||||||
Medical condition: We will investigate the effect of regularly scheduled administration of paracetamol on Quality of life, daily functioning, care dependency, pain, change in challenging behaviour and antipsychotic m... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001328-21 | Sponsor Protocol Number: ABR65448 | Start Date*: 2019-01-08 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Chronotherapy with aspirin for reduction of cardiovascular disease | ||
Medical condition: The medical condioton to be investigated is recurrent cardiovascular disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001950-33 | Sponsor Protocol Number: 15/0592 | Start Date*: 2018-01-19 | |||||||||||
Sponsor Name:UCL | |||||||||||||
Full Title: Methylphenidate versus placebo for fatigue in advanced cancer (MePFAC) | |||||||||||||
Medical condition: Cancer-related fatigue | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005658-37 | Sponsor Protocol Number: 2006-1 | Start Date*: 2006-07-07 | |||||||||||
Sponsor Name:Dpt. of Urology -K. Aarhus University Hospital | |||||||||||||
Full Title: A randomized, multi-center study to assess the effect of Darbepoetin alfa (Aranesp®) for the treatment of anemia in patients with advanced hormone independent prostate cancer and anaemia | |||||||||||||
Medical condition: In an open randomised, multi-center study to identify the haematopoietic response to Aranesp® (Darbepoetin 6,75 mcg/kg) administrated every fourth week compared to standard care of treatment in pat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003019-24 | Sponsor Protocol Number: 80-87200-98-1017 | Start Date*: 2021-08-18 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Effectiveness of analgesic ear drops as add-on treatment to oral analgesics in children with acute otitis media: a pragmatic randomised controlled trial | ||
Medical condition: Acute otitis media | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000632-34 | Sponsor Protocol Number: AAUH-ICU-01 | Start Date*: 2017-04-25 | ||||||||||||||||
Sponsor Name:Department of Anaesthesia and Intensive Care Medicine, Aalborg University Hospital | ||||||||||||||||||
Full Title: Handling oxygenation targets in adults with acute hypoxaemic respiratory failure in the intensive care unit: A randomised clinical trial of a lower versus a higher oxygenation target Addendum: Tri... | ||||||||||||||||||
Medical condition: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit Addendum: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006994-48 | Sponsor Protocol Number: EMPATICC-INCOR1 | Start Date*: 2022-07-25 | |||||||||||
Sponsor Name:Universitätsklinikum Essen | |||||||||||||
Full Title: Empower the Heart of Patients with Terminal Cancer using Cardiac Medicines Trial | |||||||||||||
Medical condition: Patients with terminal cancer in palliative care | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000218-23 | Sponsor Protocol Number: 131188 | Start Date*: 2015-03-26 | |||||||||||
Sponsor Name:Aarhus University Hospital, Skejby | |||||||||||||
Full Title: Concentration of Meropenem in Plasma and Subcutis in Patients on ECMO Treatment | |||||||||||||
Medical condition: Infections related to ECMO-hospitalisation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001314-25 | Sponsor Protocol Number: KIANANDR140701 | Start Date*: 2015-03-10 |
Sponsor Name:Karolinska Institutet | ||
Full Title: The effect of on demand versus continuous use of proton pump inhibitors on reflux symptoms, quality of life and self-rated health in patients with gastro-oesophageal reflux disease | ||
Medical condition: Gastrooesophageal reflux disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2015-004836-36 | Sponsor Protocol Number: HD202 | Start Date*: 2016-02-03 |
Sponsor Name:Department of Anaesthesiology and Intensive Care, University of Tartu | ||
Full Title: Dose dependent effects of dobutamine on central and regional blood flow in preterm and term neonates | ||
Medical condition: Hypoperfusion status of preterm and term newborns during the first days of life. | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: EE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021797-10 | Sponsor Protocol Number: TIS2012 | Start Date*: 2012-01-19 |
Sponsor Name:VU university medical center | ||
Full Title: A phase II randomized multicenter study on efficacy and safety of cultured autologous skin (Tiscover®) and acellular dermal matrix (AS210) in chronic (arterio-)venous ulcers | ||
Medical condition: The autologous cultured skin substitute (Tiscover) or acellular donor dermis (AS210) is applied to patients with chronic (arterio-) venous leg wounds. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001456-18 | Sponsor Protocol Number: AZIQUINE-ICU-25032020 | Start Date*: 2020-04-09 |
Sponsor Name:Nadační fond Donatio intensivistam | ||
Full Title: Azithromycin added to Hydrochloroquine in Patients Admitted to Intensive Care due to Coronavirus Disease 2019 (COVID-19) - Randomised Controlled Trial, phase III | ||
Medical condition: Severe COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-000312-28 | Sponsor Protocol Number: P170901J | Start Date*: 2019-12-18 |
Sponsor Name:APHP / DRCI | ||
Full Title: Extending time without diabetes after bariatric surgery: a randomized controlled trial comparing the metformin addition or not to standard care | ||
Medical condition: Type 2 Diabetes complete remission after Bariatric surgery under antidiabetic drug | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002411-29 | Sponsor Protocol Number: M13-045 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Open-Label Multicenter Study to Evaluate the Impact of Adalimumab on Quality of Life, Health Care Utilization and Costs of Ulcerative Colitis Subjects in the Usual Clinical Practice Setting. | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) GB (Completed) DE (Completed) BE (Completed) DK (Completed) GR (Completed) PT (Completed) AT (Completed) IE (Completed) IT (Completed) FI (Completed) CZ (Completed) SK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003582-25 | Sponsor Protocol Number: NL59128 | Start Date*: 2017-01-23 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The added effect of oral ondansetron to care-as-usual on persisting vomiting in children aged 6 months to 6 years, presenting at primary care out of hours service with acute gastro-enteritis and co... | ||
Medical condition: Gastroenteritis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005271-16 | Sponsor Protocol Number: 2010NE02 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:University of Dundee & NHS Tayside | |||||||||||||
Full Title: Does oral sodium bicarbonate therapy improve function and quality of life in older patients with chronic kidney disease and low-grade acidosis? A multicentre randomized placebo controlled trial | |||||||||||||
Medical condition: Chronic kidney disease stages 4/5 with metabolic acidosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005344-17 | Sponsor Protocol Number: CBDV_2014 | Start Date*: 2015-08-21 |
Sponsor Name:Department of Anesthesiology and Operative Intensive Care Medicine, Charité (CBF) | ||
Full Title: Oral cannabidivarin (CBDV) solution for treatment of HIV-associated neuropathic pain – a randomized, double-blind, placebo-controlled phase II study. | ||
Medical condition: Chronic painful HIV-associated neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001041-20 | Sponsor Protocol Number: F001AM0222_1 | Start Date*: 2022-10-14 |
Sponsor Name:University Hospital Wuerzburg | ||
Full Title: Prednisolone and vitamin B1, B6, and B12 in patients with Post-COVID-19-Syndrome (PC19S) – a randomized controlled trial in primary care | ||
Medical condition: Post-COVID-19-Syndrome (PC19S) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000292-83 | Sponsor Protocol Number: Tallisur | Start Date*: 2017-08-30 |
Sponsor Name:Servier Deutschland GmbH | ||
Full Title: Prospective, Multicenter, Open-label Phase IV trial of Trifluridine/Tipiracil to Evaluate the Health-related Quality of Life in Patients with Metastatic Colorectal Cancer | ||
Medical condition: Histologically or cytologically confirmed UICC stage IV carcinoma of colon or rectum with metastasis (metastatic colorectal cancer) with need for treatment due to progression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004726-28 | Sponsor Protocol Number: ILIT2Linköping-Jönköping | Start Date*: 2014-01-10 |
Sponsor Name:Allergy Centre | ||
Full Title: Double-blind randomised controlled study to down regulate allergic responses in adults with allergic rhinoconjunctivitis by using three intralymphatic injections of grass and/or birch allergen one ... | ||
Medical condition: Allergic rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
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