- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (21)
61 result(s) found for: Hope.
Displaying page 1 of 4.
EudraCT Number: 2014-002479-28 | Sponsor Protocol Number: MOL-ARDS-002 | Start Date*: 2015-09-24 | |||||||||||
Sponsor Name:Justus-Liebig University | |||||||||||||
Full Title: GM-CSF Inhalation to improve HOst defense and Pulmonary barrier rEstoration | |||||||||||||
Medical condition: Pneumonia associated Acute Respiratory Distress Syndrome (ARDS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001345-38 | Sponsor Protocol Number: UNIKINON-01/HOPE | Start Date*: 2020-04-02 | |||||||||||
Sponsor Name:Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. | |||||||||||||
Full Title: CHROLOQUINE PHOSPHATE AGAINST INFECTION BY THE NOVEL CORONAVIRUS SARS-CoV-2 (COVID-19): THE HOPE OPEN-LABEL, NON-RANDOMIZED CLINICAL TRIAL | |||||||||||||
Medical condition: Possible prevention of pneumonia from SARS-CoV-2 in patients staying home and improving symptoms of SARS-CoV-2 pneumonia in patients treated in hospital | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002751-15 | Sponsor Protocol Number: ST-001 | Start Date*: 2019-04-20 | |||||||||||
Sponsor Name:Hope Pharmaceuticals Ltd | |||||||||||||
Full Title: A Phase 3, Intravenous Sodium Thiosulfate for Acute Calciphylaxis Treatment: A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial | |||||||||||||
Medical condition: Calciphylaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009421-29 | Sponsor Protocol Number: AAA1 | Start Date*: 2009-05-14 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Non - invasive assessment of inflammatory burden in small abdominal aortic aneurysms: A USPIO - enhanced Magnetic Resonance Imaging (MRI) study | |||||||||||||
Medical condition: The thrust of this pilot study is to investigate the utility of USPIO - enhanced MR to image abdominal aortic aneurysms with the aim of highlighting focal areas of inflammation and macrophage infil... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000687-33 | Sponsor Protocol Number: HOPE | Start Date*: 2015-11-18 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Randomized placebo-controlled trial to investigate clinical efficacy, anti-inflammatory properties and safety of prednisolone in hand osteoarthritis: a proof-of-concept study | ||
Medical condition: Hand osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005657-12 | Sponsor Protocol Number: HUS277/03/2015 | Start Date*: 2016-01-21 |
Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö | ||
Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women | ||
Medical condition: Pain during Medical termination of pregnancy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017842-30 | Sponsor Protocol Number: 1 | Start Date*: 2010-09-17 |
Sponsor Name:West Hertfordshire Hospitals NHS Trust | ||
Full Title: A randomised, double-blind, placebo-controlled trial to compare the early administration of intravenous haloperidol versus placebo in the prevention and treatment of delirium in critically ill vent... | ||
Medical condition: Delirium | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011638-90 | Sponsor Protocol Number: 08082GM-A | Start Date*: 2009-11-09 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Targeting microvascular dysfunction in young hypertensive patients. | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003048-11 | Sponsor Protocol Number: GIPIT002 | Start Date*: 2014-10-24 |
Sponsor Name:GIPIT | ||
Full Title: FEcal transplant, a Dazzling debut to Eradicate colonization with eXtreme drug resistant bacteria? | ||
Medical condition: Patient harboring Extreme Drug Resistant (XDR) bacteria. Our trial try to eradicate this digestive tract colonization by performing a fecal transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002262-37 | Sponsor Protocol Number: ATP1 | Start Date*: 2004-10-27 |
Sponsor Name:Newcastle Hospitals Trust | ||
Full Title: Adenosine testing in the diagnosis of unexplained syncope: A pilot study | ||
Medical condition: Syncope | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002799-41 | Sponsor Protocol Number: SHRTRM3 | Start Date*: 2007-08-15 |
Sponsor Name:Salford Royal Hospitals Trust [...] | ||
Full Title: Iontophoresis as a possible therapy for digital ischaemia - preliminary studies in patients with scleroderma spectrum disorders | ||
Medical condition: Digital ischaemia/ulceration in patients with scleroderma-spectrum disorders | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005738-11 | Sponsor Protocol Number: CRAD001C2445 | Start Date*: 2006-08-23 |
Sponsor Name:Unidad integral de investigación en oncologia | ||
Full Title: Phase II Study of Single Agent RAD001 in Patients with Colon Cancer and Activating Mutations in the PI3KCA gene. | ||
Medical condition: Colon Cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011452-21 | Sponsor Protocol Number: | Start Date*: 2009-09-18 |
Sponsor Name:University Hospitals of Leicester NHS trust | ||
Full Title: Study of the effectiveness of Voriconazole in the treatment of Aspergillus fumigatus associated asthma | ||
Medical condition: Asthma with sensitization to aspergillus and isolation in sputum. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002970-36 | Sponsor Protocol Number: 54508 | Start Date*: 2016-06-06 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Human intestinal ischemia and reperfusion | ||
Medical condition: The participants enrolled in this study will all undergo major upper abdominal surgery (i.e. mostly Pylorus Preserving Pancreatico Duodenectomy or whipple procedure) mostly for pancreatic cancer, p... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003760-36 | Sponsor Protocol Number: HUS277/03/2015 | Start Date*: 2016-01-20 |
Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö | ||
Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women | ||
Medical condition: Pain during Medical termination of pregnancy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002306-19 | Sponsor Protocol Number: Hyp Hop | Start Date*: 2010-02-10 | |||||||||||
Sponsor Name:University of Rochester | |||||||||||||
Full Title: Double-blind, placebo-controlled, parallel group, phase III study comparing dichlorphenamide vs. placebo for the treatment of periodic paralysis | |||||||||||||
Medical condition: Patients with hyperkalemic (HYP) and hypokalemic (HOP) periodic paralysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001559-11 | Sponsor Protocol Number: 1312 | Start Date*: 2013-09-13 | |||||||||||
Sponsor Name:Herlev University Hospital | |||||||||||||
Full Title: Chemotherapy with gemcitabine, capecitabine, irinotecan and bevacizumab to patients with cholangiocarcinoma after progression on first line treatment. | |||||||||||||
Medical condition: patients with cholangiocarcinoma after progression. When patients with cholangiocarcinoma cannot be operated, we cannot cure them. The purpose of oncologic treatment is to prolong survival and to e... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005395-34 | Sponsor Protocol Number: CTC-cDDP | Start Date*: 2013-04-25 |
Sponsor Name:Erasmus MC | ||
Full Title: Prospective evaluation of the predictive value of a circulating tumor cell (CTC) sensitivity profile to Cisplatin chemotherapy in metastatic breast cancer patients | ||
Medical condition: Metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001362-32 | Sponsor Protocol Number: Prot-06032007 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:University Hospitals Of Leicester NHS Trust | |||||||||||||
Full Title: The use of non-ionic contrast media to clear corneal scars | |||||||||||||
Medical condition: Will plan to investigate patients who would benefit from cataract surgery but whom have corneal scarring which would make surgery difficult. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004226-16 | Sponsor Protocol Number: ACOT 2.0 | Start Date*: 2008-10-07 | |||||||||||
Sponsor Name:Carbylan BioSurgery, Inc. | |||||||||||||
Full Title: A prospective, multi-center, randomized, controlled, single-blinded study to evaluate the safety and efficacy of AdvaCoat Mx sinus gel for treatment of chronic rhinosinusitis without nasal polyps. | |||||||||||||
Medical condition: Subjects with chronic rhinosinusitis without nasal polyps, who have not had previous sinus surgery might be eligible for participation in this trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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