- Trials with a EudraCT protocol (526)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (58)
526 result(s) found for: Prednisolone.
Displaying page 1 of 27.
EudraCT Number: 2004-002783-24 | Sponsor Protocol Number: MEC02/007 PREDICT | Start Date*: 2006-05-25 |
Sponsor Name:AMC Medical research BV | ||
Full Title: Prednisolone versus Dexamethasone in Chronic inflammatory demyelinating polyradiculoneuropathy Trial; PREDICT-trial | ||
Medical condition: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an immune-mediated disorder. CIDP is characterised by motor and/or sensory symptoms and signs in more than one limb, developing o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003307-36 | Sponsor Protocol Number: LWH0606 | Start Date*: 2005-12-08 |
Sponsor Name:University of Liverpool/Liverpool Women's Hospital | ||
Full Title: A randomised controlled trial of prednisolone for women with recurrent miscarriage and high levels of uNK cells in the endometrium | ||
Medical condition: Idopathic recurrent miscarriage | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000520-14 | Sponsor Protocol Number: NL46653 | Start Date*: 2014-07-31 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Prednisolone addition for atients with recent onset psychotic disorder: the role of immune-modulating strategies in the treatment of psychosis. | ||
Medical condition: Schizophrenia, schizophreniphorm disorder, schizoaffective disorder, psychosis NOS. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) BE (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2005-002138-36 | Sponsor Protocol Number: UHL9927 | Start Date*: 2006-02-24 |
Sponsor Name:University Hospital of Leicester NHS Trust | ||
Full Title: Randomised placebo controlled trial of low dose prednisolone for 3-years in subjects with chronic obstructive pulmonary disease with a sputum eosinophilia | ||
Medical condition: Chronic obstructive pulmonary disease with sputum eosinophilia>3% | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000902-30 | Sponsor Protocol Number: SB-999920/040 | Start Date*: 2005-12-09 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: A Study of the Pharmacodynamic Effects of Prednisolone on Whole Blood Protein and Gene Expression in Rheumatoid Arthritis Patients | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014408-71 | Sponsor Protocol Number: 07/H0406/157 | Start Date*: 2009-10-08 |
Sponsor Name:UHL NHS Trust | ||
Full Title: Biomarkers to target antibiotic and systemic corticosteroid therapy in COPD exacerbations | ||
Medical condition: Exacerbations of chronic obstructive pulmonary disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004983-23 | Sponsor Protocol Number: 201900874 | Start Date*: 2021-01-18 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Bioequivalence study of prednisolone and dexamethasone: corticosteroids revisited | ||
Medical condition: This study does not investigate a medical condition and is performed in healthy volunteers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001953-27 | Sponsor Protocol Number: 9321 | Start Date*: 2004-12-13 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: The Pharmacokinetics of Systemic Corticosteriods in Refractory Asthma | ||
Medical condition: Severe, refractory asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003978-13 | Sponsor Protocol Number: M16-852 | Start Date*: 2019-09-17 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Upadacitinib in Subjects with Giant Cell Arteritis: Select-GCA | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) AT (Completed) DE (Restarted) PT (Ongoing) GR (Ongoing) HU (Ongoing) FR (Ongoing) BE (Ongoing) ES (Ongoing) NL (Ongoing) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020369-26 | Sponsor Protocol Number: 101JC404 | Start Date*: 2010-11-29 | |||||||||||
Sponsor Name:Biogen Idec | |||||||||||||
Full Title: High-Dose Corticosteroids for Immune Reconstitution Inflammatory Syndrome in Patients Who Develop Progressive Multifocal Leukoencephalopathy on Natalizumab | |||||||||||||
Medical condition: Immune Reconstitution Inflammatory Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000560-17 | Sponsor Protocol Number: 0146366 | Start Date*: 2008-09-16 | |||||||||||
Sponsor Name:UMC Utrecht, Julius Center for Health Sciences and Primary Care | |||||||||||||
Full Title: Prednisolone Rhinosinusitis Efficacy Trial (PRET) study | |||||||||||||
Medical condition: patients (> 18 years) with rhinosinusitis-like symptoms lasting for at least 5 days. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002084-27 | Sponsor Protocol Number: cro-725 | Start Date*: 2007-10-02 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: The pharmacokinetics and anti-inflammatory effects of prednisolone in severe asthma. | |||||||||||||
Medical condition: This study is designed to look why patients with severe asthma fail to respond to oral corticosteroids in the same way as patients with non-severe disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005032-35 | Sponsor Protocol Number: ATL2502/020/CL | Start Date*: 2005-10-11 |
Sponsor Name:Alizyme Therapeutics Limited | ||
Full Title: A Multicentre, Randomised, Double-Blind, Double-Dummy, Active Comparator Controlled, Parallel Group Study of COLAL PRED® in the Treatment of Moderate Acute Ulcerative Colitis. | ||
Medical condition: Moderate acute ulcerative colitis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) CZ (Completed) HU (Completed) DK (Completed) ES (Ongoing) BE (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022489-29 | Sponsor Protocol Number: RG_08-015 | Start Date*: 2011-04-05 |
Sponsor Name:The University of Birmingham [...] | ||
Full Title: Long-term tapering versus standard prednisolone (steroid) therapy for the treatment of the initial episode of childhood nephrotic syndrome: national multicentre randomised double blind trial | ||
Medical condition: Childhood nephrotic syndrome | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002295-41 | Sponsor Protocol Number: PR2100 | Start Date*: 2009-01-29 |
Sponsor Name:The University of Birmingham | ||
Full Title: A randomised phase II/III study of Docetaxel plus Prednisolone vs. Docetaxel plus Prednisolone plus Zoledronic acid vs. Docetaxel plus Prednisolone plus Strontium-89 vs. Docetaxel plus Prednisolo... | ||
Medical condition: Hormone refractory Prostate Cancer (HRPC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-006018-16 | Sponsor Protocol Number: | Start Date*: 2006-02-27 |
Sponsor Name:Royal Marsden Hospital | ||
Full Title: A Randomised Phase III Trial Of Low Dose DailyDexamethasone Versus Intermittent Dexamethasone Versus Prednisolone In Hormone Refractory Prostate Cancer | ||
Medical condition: Hormone refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001474-12 | Sponsor Protocol Number: GRAY07 | Start Date*: 2006-05-16 |
Sponsor Name:Research and Innovation Services | ||
Full Title: A Proof Of Concept Study to Investigate the Clinical, Histological And Molecular Predictors of Response to Oral and Intranasal Corticosteroid in Nasal Polyposis | ||
Medical condition: Nasal Polyposis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003476-39 | Sponsor Protocol Number: RG_12-188 | Start Date*: 2012-12-04 |
Sponsor Name:The University of Birmingham [...] | ||
Full Title: Short course daily prednisolone therapy at the time of upper respiratory tract infection in children with relapsing steroid sensitive nephrotic syndrome; the PREDNOS 2 study. | ||
Medical condition: Relapsing steroid sensitive nephrotic syndrome | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2005-003593-16 | Sponsor Protocol Number: D4200C00055 | Start Date*: 2005-11-23 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A phase II, double-blind, placebo-controleed, randomised study to assess the efficacy and safety of docetaxel (Taxotere)/ prednisolone/ ZD6474 vs. docetaxel/ prednisolone/ placebo in patients with ... | ||
Medical condition: Hormone refractory prostate cancer (HRPC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Completed) HU (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014292-52 | Sponsor Protocol Number: GRIM1002 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:Imperial College NHS trust | |||||||||||||
Full Title: Tacrolimus vs prednisolone for the treatment of nephrotic syndrome secondary to minimal change disease: A Randomised Control Trial | |||||||||||||
Medical condition: Nephrotic syndrome with lesion minimal change glomerulonephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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