- Trials with a EudraCT protocol (908)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
908 result(s) found for: Steroids.
Displaying page 9 of 46.
| EudraCT Number: 2004-005174-23 | Sponsor Protocol Number: CAVA2Dec04 | Start Date*: 2005-04-11 |
| Sponsor Name:NHS Grampian | ||
| Full Title: Is smooth muscle mitogenesis down regulated by platelet inactivation with combination antiplatelet therapy after angioplasty for claudication? | ||
| Medical condition: Intermittent claudication = stenosis of superficial femoral artery requiring percutaneous angioplasty | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003561-13 | Sponsor Protocol Number: cro488 | Start Date*: 2006-12-04 |
| Sponsor Name:imperial college | ||
| Full Title: Reversal of steroid insensitivity in COPD by theophylline | ||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011173-32 | Sponsor Protocol Number: RR09/8877 | Start Date*: 2009-07-07 | |||||||||||
| Sponsor Name:University of Leeds | |||||||||||||
| Full Title: Treating painful hand osteoarthritis using low dose oral prednisolone- assessing short-term pain and imaging outcomes | |||||||||||||
| Medical condition: painful osteoarthritis of the hands | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001212-30 | Sponsor Protocol Number: GW/MB/42964 | Start Date*: 2013-07-04 |
| Sponsor Name: | ||
| Full Title: Modulation of immune function by parenteral fish oil in patients with Crohn’s disease and high inherent Tumor Necrosis Factor-alfa production, a randomized, single blinded, cross-over study | ||
| Medical condition: Crohn's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001770-30 | Sponsor Protocol Number: 2020COVID-19TCZ | Start Date*: 2020-04-21 | |||||||||||
| Sponsor Name:CHU AMBROISE PARE | |||||||||||||
| Full Title: COVID 19: Experimental use of tocilizumab (Roactemra®) in severe SARS-CoV-2 related pneumonia. | |||||||||||||
| Medical condition: viral pneumonia caused by the new coronavirus (SARS-CoV-2) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-001231-29 | Sponsor Protocol Number: 2005-01-02 | Start Date*: 2005-09-08 |
| Sponsor Name:Dept of Transplantation Surgery B 56, Karolinska University Hospital, Huddinge | ||
| Full Title: A PROSPECTIVE, RANDOMISED, PLACEBO CONTROLLED, MULTI-CENTER STUDY OF THE EFFICACY AND SAFETY OF RITUXIMAB AS INDUCTION THERAPY TOGETHER WITH TACROLIMUS, MYCOPHENOLATE MOFETIL AND STEROIDS FOR PATI... | ||
| Medical condition: Chronic renal failure patients who are receiving a kidney transplant. Different immunosuppressive protocls are awailable. However, current strategies for the medical management of transplant patie... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001090-10 | Sponsor Protocol Number: D5892L00002 | Start Date*: 2005-08-17 |
| Sponsor Name:AstraZeneca AB, AstraZeneca Sverige | ||
| Full Title: A randomised, double blind, double dummy, multicentre phase III study comparing the efficacy of budesonide/formoterol (Symbicort® forte Turbuhaler®) and oral prednisolone + formoterol (Oxis® Turbuh... | ||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) FI (Completed) DK (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005008-15 | Sponsor Protocol Number: Okhn1001 | Start Date*: 2006-11-08 | |||||||||||
| Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | |||||||||||||
| Full Title: Exploratory study of intravitreal clindamycin and dexamethasone in the treatment of acute toxoplasma chorioretinitis associated vitritis | |||||||||||||
| Medical condition: Vitritis secondary to acute toxoplasma chorioretinitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000543-27 | Sponsor Protocol Number: 19852012 | Start Date*: 2012-04-23 |
| Sponsor Name:AMC | ||
| Full Title: A Proof of Concept Study to Determine the Local Delivery and Efficacy of Intravenously Injected PEG-Liposomal Prednisolone Sodium Phosphate (Nanocort®) in Atherosclerotic Tissue in Subjects with Pe... | ||
| Medical condition: Vessel wall inflammation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002173-22 | Sponsor Protocol Number: 201800406 | Start Date*: 2018-12-04 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Anti-inflammatory effects of tiotropium in patients with stable COPD | ||
| Medical condition: Chronic obstructive pulmonary disease (COPD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004222-93 | Sponsor Protocol Number: GPE 02 | Start Date*: 2006-11-28 |
| Sponsor Name:Curalogic A/S | ||
| Full Title: Assessment of the Maximal Tolerated Dose of a Microencapsulated Grass (Phleum pratense) Pollen Extract (MGPE) in Subjects with Grass Pollen Allergy in a Randomized, Double-Blind, Placebo-Controlled... | ||
| Medical condition: Treatment of seasonal allergic rhinitis to grass pollen. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000407-84 | Sponsor Protocol Number: Beta-Dexa-Caudal | Start Date*: 2016-04-20 |
| Sponsor Name:Enrique Bárez Hernandez | ||
| Full Title: Efficacy and safety of epidural administration of betamethasone and dexamethasone by caudal route for the treatment of radicular pain: randomized clinical trial. | ||
| Medical condition: radiculalgia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003707-37 | Sponsor Protocol Number: 291-416 | Start Date*: 2007-05-25 | |||||||||||
| Sponsor Name:PDL BioPharma, Inc | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Visilizumab in Subjects with Intravenous Steroid-Refractory Ulcerative Colitis | |||||||||||||
| Medical condition: Intravenous Steroid-Refractory Ulcerative Colitis (IVSR-UC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004486-26 | Sponsor Protocol Number: IGG-SN-MAB2 | Start Date*: 2008-10-07 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Efficacy of monoclonal anti CD 20 antibodies in steroid and cyclosporin dependent nephrotic syndrome in children | |||||||||||||
| Medical condition: Nephrotic Syndrome | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| 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: 2004-002547-27 | Sponsor Protocol Number: OP/CD001 | Start Date*: 2005-09-03 |
| Sponsor Name:University of Bristol | ||
| Full Title: Combined Immunosuppression and Radiotherapy in Thyroid Eye Disease | ||
| Medical condition: Thyroid Eye Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001307-16 | Sponsor Protocol Number: SIC | Start Date*: 2020-04-01 |
| Sponsor Name:Fundación para la Investigación Biomédica Hospital Ramón y Cajal | ||
| Full Title: Efficacy and Safety of corticoids in patients with adult respiratory distress syndrome (ARDS) secondary to COVID-19. | ||
| Medical condition: Adult respiratory distress syndrome (ARDS) secondary to SARS-CoV-2 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000695-40 | Sponsor Protocol Number: Final Version 2, 7 June 2005 | Start Date*: 2005-09-27 |
| Sponsor Name:University of Nottingham | ||
| Full Title: A randomised trial of aminosalicylate withdrawal in patients with ulcerative colitis in established remission on combination treatment of azathioprine (or 6−mercaptopurine) and an aminosalicylate | ||
| Medical condition: The medical condition is Ulcerative Colitis. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| 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: 2007-004538-18 | Sponsor Protocol Number: RPE 07 | Start Date*: 2007-12-19 |
| Sponsor Name:Curalogic A/S | ||
| Full Title: A randomized doble-blind placebo-controlled study to assess the safety in a one-year of orally administered microencapsulated ragweed pollen extract | ||
| Medical condition: Patients with ragweed pollen allergy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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