- Trials with a EudraCT protocol (157)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
157 result(s) found for: Palliative care.
Displaying page 1 of 8.
EudraCT Number: 2006-007053-51 | Sponsor Protocol Number: 003/APR06 | Start Date*: 2007-07-02 | ||||||||||||||||
Sponsor Name:Gloucestershire Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: Diamorphine or alfentanil for subcutaneous use in hospice in-patients | ||||||||||||||||||
Medical condition: Palliative Care | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000080-85 | Sponsor Protocol Number: 17-245 | Start Date*: 2018-11-29 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Pilot study of the pharmacokinetic profile of paracetamol subcutaneously versus intravenously in patients receiving palliative care | |||||||||||||
Medical condition: Major patients in palliative care | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016701-42 | Sponsor Protocol Number: I08014 | Start Date*: 2010-01-22 | ||||||||||||||||
Sponsor Name:CHU Limoges | ||||||||||||||||||
Full Title: Techniques anesthésiques locorégionales et qualité de vie en soins palliatifs | ||||||||||||||||||
Medical condition: palliative care Cancer pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2012-000850-75 | Sponsor Protocol Number: OZ0110110016 | Start Date*: 2012-07-18 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Clinical evaluation of the efficacy of methylnaltrexone in resolving constipation induced by different opioid subtypes combined with laboratory analysis of immunomodulatory and antiangiogenic effec... | |||||||||||||
Medical condition: patients receiving palliative care suffering from opioid induced constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002080-27 | Sponsor Protocol Number: KPS 2008-01 | Start Date*: 2008-08-06 | ||||||||||||||||
Sponsor Name:Greater Glasgow Health Board/University of Glasgow | ||||||||||||||||||
Full Title: A randomised, double-blind controlled trial of ketamine versus placebo in conjunction with best pain management in neuropathic pain in cancer patients | ||||||||||||||||||
Medical condition: Patients who have neuropathic pain related to cancer and/or treatment for cancer (surgical, chemotherapy or radiotherapy) which has resulted in neuropathic pain. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2015-000202-20 | Sponsor Protocol Number: RC-P0041 | Start Date*: 2015-06-22 | |||||||||||||||||||||||||||||||
Sponsor Name:Groupement des Hôpitaux de l’Institut Catholique de Lille (GHICL) | |||||||||||||||||||||||||||||||||
Full Title: Effect and tolerance of ketamine's subcutaneous bolus during painful care, refractory of bedsore, ulcer, vascular wound care in palliative care units. | |||||||||||||||||||||||||||||||||
Medical condition: Patients’ palliative care for bedsores, ulcers or vascular wounds, which are general characteristics of the patient population that will be included: usually elderly, undernourished and of multiple... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000502-40 | Sponsor Protocol Number: RHM CAN0380 | Start Date*: 2005-05-13 |
Sponsor Name:Southampton University Hospitals Trust | ||
Full Title: A thematic analysis of semi-structured interviews using a phenomenological approach into palliative care patients experiences of change in "fatigue" following treatment with methylphenidate – an ex... | ||
Medical condition: Patients with cancer in palliative stage of their illness. Suffering from fatigue with or without decreased concentration, depression or drowsiness, who feel their fatigue is severe enough to decre... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007610-10 | Sponsor Protocol Number: 11500005 | Start Date*: 2009-01-13 | |||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||
Full Title: Prevention of constipation during treatment with opioids: magnesiumoxide versus macrogol/elektrolytes | |||||||||||||
Medical condition: Palliative care cancer patients starting with opioids | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001128-36 | Sponsor Protocol Number: IIBSP-PAI-2011-36 | Start Date*: 2012-09-21 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: Integral care program with or without palliative chemotherapy in patients with advanced cancer: multicentre randomized clinical trial. | ||
Medical condition: Patients with advanced cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002699-13 | Sponsor Protocol Number: EK 070/05 | Start Date*: 2005-11-25 |
Sponsor Name:Department of Palliative Medicine, RWTH Aachen | ||
Full Title: Modafinil in der Behandlung von Müdigkeit bei Tumorpatienten - eine randomisierte doppelblinde N=1 Studie | ||
Medical condition: advanced cancer disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-004789-36 | Sponsor Protocol Number: 173-01 | Start Date*: 2022-06-29 |
Sponsor Name:Universität Heidelberg | ||
Full Title: Randomized, controlled trial of the use of intranasal midazolam for the treatment of terminal agitation in palliative care patients | ||
Medical condition: Terminal agitation in the final phase | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000142-18 | Sponsor Protocol Number: 1.0 | Start Date*: 2018-05-09 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Feasibility and pharmacodynamics of subcutaneously given combination of dexmedetomidine and ketamine infusion in ALS patients receiving palliative care | |||||||||||||
Medical condition: Amyotrophic lateral sclerosis (ALS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004282-25 | Sponsor Protocol Number: CHUBX2014/10 | Start Date*: 2015-03-25 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Subcutaneous route and pharmacology of metoclopramide - SOPHA-Méto | ||
Medical condition: Digestive disorder (Nausea and vomiting) in palliative care and oncology | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000927-29 | Sponsor Protocol Number: NL60405.100.17 | Start Date*: 2017-07-31 |
Sponsor Name:Catharina Ziekenhuis | ||
Full Title: Repetitive electrostatic pressurised intraperitoneal aerosol chemotherapy with oxaliplatin as a palliative monotherapy for isolated unresectable colorectal peritoneal metastases: protocol of a mult... | ||
Medical condition: Isolated unresectable colorectal peritoneal metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002282-19 | Sponsor Protocol Number: MENAC-2017-03 | Start Date*: 2016-05-17 |
Sponsor Name:Norwegian University of Science and technology | ||
Full Title: A randomised, open-label trial of a Multimodal Intervention (Exercise, Nutrition and Anti-inflammatory Medication) plus standard care versus standard care alone to prevent / attenuate cachexia in a... | ||
Medical condition: cachexia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004377-44 | Sponsor Protocol Number: Ambroxpall | Start Date*: 2021-08-24 |
Sponsor Name:Med. Univ. Wien, Innere Med. I, Abt. f. Palliativmedizin | ||
Full Title: Ambroxol inhalation for mucus clearance in palliative care patients - a randomized placebo-controlled double-blind pilot study. | ||
Medical condition: cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001010-34 | Sponsor Protocol Number: G-LUCAS | Start Date*: 2011-11-08 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: A randomized, placebo-controlled, double-blind multicenter phase II study to investigate the protectivity and efficacy of Metformin against steatosis in combination with FOLFIRI and Cetuximab in su... | ||
Medical condition: first-line palliative treated, KRAS-Wild-Type, metastatic colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-001938-42 | Sponsor Protocol Number: UCL-ONCO2011-01 | Start Date*: 2012-01-24 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Randomized Phase II Study of CABAZITAXEL versus METHOTREXATE in patients with recurrent or metastatic squamous cell carcinoma of the head and neck previously treated with platinum-based therapy | ||
Medical condition: To evaluate the efficacy of cabazitaxel in patients with palliative head and neck previously treated with platinum-based therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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