- Trials with a EudraCT protocol (145)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
145 result(s) found for: Vitamin D3.
Displaying page 4 of 8.
EudraCT Number: 2011-003699-34 | Sponsor Protocol Number: QA343 | Start Date*: 2012-03-02 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: Feasibility study including a double blind (C)controlled study and an open label (C) controlled study for a larger randomised trial measuring the effect of oral vitamin D (I) on morbidity and morta... | ||
Medical condition: The aim of vitamin D supplementation is to increase circulating 25(OH) vitamin D level in the general population. The aim of the main trial for which this is a feasibility study is to determine whe... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003573-10 | Sponsor Protocol Number: 2012GA03 | Start Date*: 2013-11-07 | |||||||||||
Sponsor Name:University of Dundee & NHS Tayside | |||||||||||||
Full Title: Can Vitamin D supplementation improve Hepatitis C cure rates: A pilot multicentre randomised controlled clinical trial | |||||||||||||
Medical condition: Hepatitis C virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005619-18 | Sponsor Protocol Number: Calcichew-4001 | Start Date*: 2015-05-05 | ||||||||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd. | ||||||||||||||||||
Full Title: A Randomized, Open-Label, 2-Way Cross-over, Phase 4 Study to Evaluate Subject Preference and Acceptability of a New Formulation of Calcichew D3 in Adult Patients Eligible for Calcium and Vitamin D ... | ||||||||||||||||||
Medical condition: Prevention and treatment of vitamin D and calcium deficiency and adjunct to specific osteoporosis treatment of patients who are at risk of vitamin D and calcium deficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001793-30 | Sponsor Protocol Number: 20200412 | Start Date*: 2020-07-01 | |||||||||||||||||||||
Sponsor Name:Copenhagen University Hospital of Bispebjerg | |||||||||||||||||||||||
Full Title: Preventing Disease Aggravation in COVID-19 by high dose Vitamin D: a randomized trial (COVIT-D) | |||||||||||||||||||||||
Medical condition: SARS-COV-2 positive patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023531-42 | Sponsor Protocol Number: 26992 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:Psykiatrien i Region Syddanmark | |||||||||||||
Full Title: The role of vitamin D supplementation on symptoms in patients treated for depression. A double-blind randomized trial. | |||||||||||||
Medical condition: Depression as defined by fulfilled ICD-10 criteria for diseases F32.1-3, F33.1-3. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003546-16 | Sponsor Protocol Number: 1.2 | Start Date*: 2014-03-20 |
Sponsor Name:Medizinische Universität Wien, Klin. Abt. für Endokrinologie & Stoffwechsel, Universitätsklinik für Innere Medizin III | ||
Full Title: The Link between Obesity And Vitamin D in bariatric patients with omega-loop bypass surgery: a randomized controlled, double-blinded clinical supplementation trial - LOAD | ||
Medical condition: The aim of the study is to increase vitamin D concentrations respectively to keep it on high level by supplementing with cholecalciferol in a different dose regime, and to improve the overall healt... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-024150-10 | Sponsor Protocol Number: OPO-ALD-CHF-301 | Start Date*: 2011-08-04 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd. | |||||||||||||
Full Title: A-15 week, double-blind, randomized, active-controlled, multicenter study to evaluate the efficacy and safety of Alendronate plus Vitamin D3 in women with osteoporosis | |||||||||||||
Medical condition: Treatment of postmenopausal osteoporosis in patients at risk of vitamin D insufficiency. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024588-42 | Sponsor Protocol Number: 2010124801 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Vitamin D supplementation and male infertility: a randomized double blinded clinical trial | |||||||||||||
Medical condition: Male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015940-40 | Sponsor Protocol Number: VIDI-P | Start Date*: 2010-03-11 |
Sponsor Name:Helsingin ja uudenmaan sairaanhoitopiiri | ||
Full Title: Vitamin-D intervention pilotti | ||
Medical condition: Tutkittavat ovat terveitä vastasyntyneitä iältään 2 viikosta 3 kuukauteen. | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003994-23 | Sponsor Protocol Number: DagainstGVH | Start Date*: 2021-09-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: Role of Vitamin D in GVHD prophylaxis in patients undergoing allogeneic stem cell transplantation. Randomized single-center pilot study | |||||||||||||
Medical condition: Treatment of acute and chronic graft versus host disease (GVHD) after allogeneic donor hematopoietic stem cell transplantation in adult patients with haematological diseases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001903-17 | Sponsor Protocol Number: HMos-012020 | Start Date*: 2020-06-10 |
Sponsor Name:HOSPITAL UNIVERISTARIO DE MOSTOLES | ||
Full Title: A randomized clinical trial (IIIb) of eficacy of a single dose of Tocilizumab or a combination of Tocilizumab plus Vitamin D (single i.m. dose) for the treatment of the COVID-19 hyperimmune complic... | ||
Medical condition: COVID INFECTION IS A MILD FLU LIKE CONDITION WITH MILD FEVER, DRY COUGH, WIDESPREAD TENDERNESS AND OLFACTORY DISFUNCTION FOLLOWED BY A SERIOUS SITUATION IN SOME 20% OF PATIENTS WITH OVERT FEVER, MA... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004512-11 | Sponsor Protocol Number: FJD-VITDAMI-14-01 | Start Date*: 2015-08-06 |
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA FJD | ||
Full Title: Multicenter, randomized, double-blind, placebo-controlled study to evaluate the effect of vitamin D on ventricular remodeling in patients with acute myocardial infarction: Test VITDAMI (Vitamin D i... | ||
Medical condition: Acute myocardial infarction with ST segment elevation anterior | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002274-28 | Sponsor Protocol Number: COVID-VIT-D | Start Date*: 2020-05-19 | |||||||||||
Sponsor Name:Fundación para la Investigación y la Innovación Biosanitaria del Principado de Asturias (FINBA) | |||||||||||||
Full Title: Usefulness of vitamin D on morbidity and mortality of SARS-COV-2 virus infection (Covid-19) at the Central University Hospital of Asturias | |||||||||||||
Medical condition: SARS-COV-2 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000971-34 | Sponsor Protocol Number: 01052013 | Start Date*: 2013-08-01 | |||||||||||
Sponsor Name:Jørgen Agnholt | |||||||||||||
Full Title: Mucosal immune regulation by high dose vitamin D treatment in Crohn’s disease | |||||||||||||
Medical condition: Active Crohn's Disease in colon and/or terminal ileum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003010-17 | Sponsor Protocol Number: - | Start Date*: 2011-07-07 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Randomized double-blind intervention trial to assess the efficacy of vitamin D3 supplementation vs placebo in reducing hepatic steato-inflammation and cardio-metabolic risk profile in patients affe... | |||||||||||||
Medical condition: Patients affected by type 2 diabetes and non alcoholic fatty liver disease- non alcoholic steato-hepatitis (NAFLD/NASH) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002244-42 | Sponsor Protocol Number: VITD1/08 | Start Date*: 2009-07-03 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Does 1-alpha,25-dihydroxyvitamin D3 (calcitriol) enhance corticosteroid activity in steroid refractory asthma? A randomised control trial to test whether active vitamin D can improve the clinica... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012049-46 | Sponsor Protocol Number: IEO S480/209 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Phase III, randomized, double blind trial on Vitamin D supplementation for resected stage II melanoma patients. | |||||||||||||
Medical condition: melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003575-11 | Sponsor Protocol Number: VitaminD&TT | Start Date*: 2013-03-05 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Innere Medizin | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled trial to evaluate the effects of vitamin D supplementation on androgen levels in hypogonadal men | |||||||||||||
Medical condition: Male hypogonadism (total testosterone <3ng/ml) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001254-25 | Sponsor Protocol Number: CMC-P003 | Start Date*: 2006-03-06 |
Sponsor Name:CMC Contrast AB | ||
Full Title: Evaluation of the diagnostic efficacy of CMC-001 (manganese chloride tetrahydrate) in liver MR-imaging in patients with liver metastases. A randomised, parallel group, open-label Phase II trial. | ||
Medical condition: Liver metastases. CMC - 001 is an orally administered contrast medium containing manganese chloride tetrahydrate (MnCl2 tetrahydrate) as the active imaging substance. Manganese is absorbed by the h... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001449-42 | Sponsor Protocol Number: VITDCirrhosis2012 | Start Date*: 2014-10-03 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Kl. Abt. f. Endokrinoloie u. Stoffwechsel & Kl. Abt. f. Gastroenterologie u. Hepatologie | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled trial to evaluate vitamin D supplementation on serum 25 hydroxy- vitamin D level in cirrhotic patients | |||||||||||||
Medical condition: decompensated and compensated liver cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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