- Trials with a EudraCT protocol (63)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
63 result(s) found for: MIBE.
Displaying page 1 of 4.
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 (Trial now transitioned) AT (Completed) DE (Trial now transitioned) PT (Trial now transitioned) GR (Completed) HU (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014532-37 | Sponsor Protocol Number: JU-AMG-403-1-1 | Start Date*: 2011-01-13 |
Sponsor Name:Universitätsklinikum Schleswig-Holstein | ||
Full Title: Effekte von oraler Cortisol oder Propranolol-Gabe auf die Verarbeitung alkoholbezogener Schlüsselreize, den Schlaf und das Rückfallrisiko von alkoholabhängigen Patienten (Copro-Studie). | ||
Medical condition: alkohol dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003557-27 | Sponsor Protocol Number: SA-388-4-1 | Start Date*: Information not available in EudraCT |
Sponsor Name:Dean of the Medical Faculty (University of Bonn) | ||
Full Title: Covered Transjugular Intrahepatic Portosystemic Stent Shunt versus Optimized medical Treatment for the Secondary Prevention of Variceal Bleeding in Cirrhosis | ||
Medical condition: liver cirrhosis; esophageal (variceal) bleeding | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002602-36 | Sponsor Protocol Number: KKSH-127 | Start Date*: 2016-06-21 |
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | ||
Full Title: Efficacy and safety of high dose glucocorticosteroid treatment for idiopathic sudden sensorineural hearing loss (HODOKORT) | ||
Medical condition: Idiopathic sudden sensorineural hearing loss | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006438-82 | Sponsor Protocol Number: 001 | Start Date*: 2009-06-15 |
Sponsor Name:Odense Universitetshospital, Nyremedicinsk Afd. Y | ||
Full Title: Vitamin D og kronisk nyreinsufficiens | ||
Medical condition: Investigating the effects of treatment with not activated vitamin D (cholecalciferol) in chronic kidney disease petients with vitamin D deficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015649-21 | Sponsor Protocol Number: Kamycheva/2009/1 | Start Date*: 2009-10-21 |
Sponsor Name:Medical clinic, University Hospital of North Norway | ||
Full Title: Immunmodulating and clinical effect of vitamin D onthe induction of remission in the patients with moderate to severe ulcerative colitis under the treatment with Infliximab. | ||
Medical condition: Ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002363-15 | Sponsor Protocol Number: EVITA | Start Date*: 2015-02-13 |
Sponsor Name:University Medical Center of the Johannes Gutenberg University Mainz | ||
Full Title: EVITA Trial: Effect of VItamin D as add-on Therapy for vitamin D insufficient patients with severe Asthma: a randomized, double-blind, placebo-controlled trial. | ||
Medical condition: severe asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-023189-27 | Sponsor Protocol Number: RG-10-179 | Start Date*: 2011-01-20 |
Sponsor Name:University of Birmingham | ||
Full Title: The pharmacogenetics of vitamin D response in tuberculosis | ||
Medical condition: Tuberculosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005903-25 | Sponsor Protocol Number: SC12267-4-2008 | Start Date*: 2009-01-08 | |||||||||||
Sponsor Name:4SC AG | |||||||||||||
Full Title: Exploratory, open-label study to demonstrate efficacy, safety and tolerability of SC12267 (35 mg) in patients with inflammatory bowel disease (Crohn’s disease and ulcerative colitis) | |||||||||||||
Medical condition: inflammatory bowel disease (Crohn’s disease and ulcerative colitis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006793-26 | Sponsor Protocol Number: 06-03/DPI Salmeterol_50 | Start Date*: 2007-09-20 | |||||||||||
Sponsor Name:mibe GmbH Arzneimittel | |||||||||||||
Full Title: Randomised, double-blind, double-dummy, cross-over trial comparing salmeterol 50 µg b.i.d. via a novel DPI versus salmeterol 50 µg b.i.d. via Diskus in adult patients with persistent asthma | |||||||||||||
Medical condition: Adult patients with stable persistent asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002785-20 | Sponsor Protocol Number: EVIDIMS | Start Date*: 2011-09-19 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Efficacy of Vitamin D Supplementation in relapsing-remitting Multiple Sclerosis | ||
Medical condition: Multiple Sclerosis and Clinical isolated Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-003514-40 | Sponsor Protocol Number: TromsøEndo-2013-1 | Start Date*: 2013-09-17 |
Sponsor Name:University Hospital of North Norway | ||
Full Title: The effect of vitamin D supplementation on cardiovascular risk factors in subjects with low serum 25-hydroxyvitamin D levels | ||
Medical condition: subjects with serum 25-hydroxyvitamin D < 35 nmol/L will be included and the effect of vitamin D supplementation versus placebo tested regarding cardiovascular risk factors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005875-38 | Sponsor Protocol Number: TRINITY | Start Date*: 2022-09-20 |
Sponsor Name:LMU Klinikum der Universität München | ||
Full Title: A multicenter, randomized, double-blind, placebo-controlled TRial evaluating Immunosuppressive treatment in patients with chronic virus-Negative Inflammatory cardiomyopaThY (TRINITY trial) | ||
Medical condition: Patients with biopsy-proven virus-negative inflammatory dilated or non-dilated left ventricular cardiomyopathy and persistent deterioration of cardiac function despite optimal medical treatment (OM... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-007073-75 | Sponsor Protocol Number: 07-01/DPI Fluticason_250 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:mibe GmbH Arzneimittel | |||||||||||||
Full Title: Randomised, double-blind, double-dummy, parallel trial comparing a novel DPI with 250 µg fluticasone versus Flutide® 250 Diskus® in patients with persistent asthma | |||||||||||||
Medical condition: Persistent Asthma in adults | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003239-31 | Sponsor Protocol Number: HOVIR_700 | Start Date*: 2014-03-14 |
Sponsor Name:HOV GmbH | ||
Full Title: A randomised, placebo-controlled, single-centre, double-blind study to evaluate the efficacy, safety and tolerability of topically applied piroxicam gel in patients with recurrent herpes labialis | ||
Medical condition: Recurrent Herpes labialis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023122-21 | Sponsor Protocol Number: PB002 | Start Date*: 2011-11-08 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: Pro-Bono 2- A prospective study of loss of bone mineral density in patients with HIV over time: implications for clinical practice and therapeutic options: Vitamin D sub study. | ||||||||||||||||||
Medical condition: HIV | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003395-72 | Sponsor Protocol Number: VitD@BPPV | Start Date*: 2016-11-29 |
Sponsor Name:Hospital of the University of Munich | ||
Full Title: Vitamin D in secondary prevention of benign paroxysmal positional vertigo: a prospective, multicenter, randomized, placebo-controlled, double-blind study (VitD@BPPV) | ||
Medical condition: The main symptoms of Benign Paroxysmal Positional Vertigo (BPPV) are brief, in part strong attacks of rotatory vertigo lasting seconds. These attacks can be provoked by reclination of the head or t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000133-13 | Sponsor Protocol Number: 2020-01131 | Start Date*: 2022-05-05 | |||||||||||
Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
Full Title: Glucocorticoid enhancement of food exposure therapy in Binge Eating Disorder | |||||||||||||
Medical condition: Binge-Eating-Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001682-12 | Sponsor Protocol Number: MYOFLAME-19 | Start Date*: 2023-06-16 | ||||||||||||||||
Sponsor Name:Goethe University Frankfurt | ||||||||||||||||||
Full Title: Randomised placebo controlled clinical trial of efficacy of MYOcardial protection with postacute inFLAMmatory cardiac involvEment due to COVID-19 (MYOFLAME-19) | ||||||||||||||||||
Medical condition: Inflammatory cardiovascular involvement due to COVID-19, defined by Cardiovascular magnetic resonance imaging | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000502-30 | Sponsor Protocol Number: DKFZ-2019-001 | Start Date*: 2020-03-26 | |||||||||||||||||||||
Sponsor Name:German Cancer Research Center (DKFZ) | |||||||||||||||||||||||
Full Title: Personalized Vitamin D Supplementation for Reducing or Preventing Fatigue and Enhancing Quality of Life of Patients with Colorectal Tumor: Randomized Intervention Trial | |||||||||||||||||||||||
Medical condition: Fatigue in patients with colorectal cancer (ICD codes C18-C20 and C21.8) within 12 months after a colorectal cancer therapy (surgery, chemotherapy and/ or radiation) and not optimal vitamin D status | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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