- Trials with a EudraCT protocol (145)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
145 result(s) found for: Vitamin D3.
Displaying page 1 of 8.
EudraCT Number: 2012-003217-33 | Sponsor Protocol Number: ViDImmun | Start Date*: 2013-02-04 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Immunological response of a single dose of 100,000 I.U. of cholecalciferol (vitamin D3) | |||||||||||||
Medical condition: relative vitamin D3 deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006789-19 | Sponsor Protocol Number: NephroD_2021 | Start Date*: 2022-05-16 | |||||||||||
Sponsor Name:USK w Opolu | |||||||||||||
Full Title: Efficacy comparison of two doses of vitamin D3 in critically ill patients undergoing continuous renal replacement therapy - NephroD | |||||||||||||
Medical condition: Vitamin D3 deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021756-26 | Sponsor Protocol Number: SOMAQ | Start Date*: 2010-11-08 |
Sponsor Name:VG Region, Sahlgrenska sjukhuset, Hudkliniken, Göteborg | ||
Full Title: Behandlingseffekt av UV ljus jämfört med peroralt D vitamin på D-vitaminnivån hos somaliska kvinnor | ||
Medical condition: - Studera effekten på serum vitamin D-nivåerna före och efter vitamin D behandling av vuxna somaliska kvinnor boende i Sverige. - Jämföra serum vitamin D-nivåerna mellan behandling med peroralt vi... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000200-38 | Sponsor Protocol Number: VitDM3BH | Start Date*: 2021-06-13 |
Sponsor Name:University Clinic of Dentistry, Medical University of Vienna | ||
Full Title: THE IMPACT OF VITAMIN D3 HIGH DOSES SUPPLEMENTATTION ON SOFT TISSUE WOUND-HEALING AFTER MANDIBULAR THIRD MOLAR (M3) REMOVAL: A PILOT STUDY | ||
Medical condition: Vitamin D insufficiency undergoing tooth extraction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003478-29 | Sponsor Protocol Number: VIDAFACT | Start Date*: 2014-03-21 |
Sponsor Name:Maria Nabal Vicuña (Paliative Care Supportive Team-Hospital Universitari Arnau de Vilanova de Lleida) | ||
Full Title: The effect on quality of life of Vitamin D administration for advanced cancer treatment. A randomized controlled trial | ||
Medical condition: The effect on quality of life of Vitamin D administration for advanced cancer treatment. A randomized controlled trial | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003954-13 | Sponsor Protocol Number: UKO-1006-2008 | Start Date*: 2008-09-30 |
Sponsor Name:Silkeborg Hospital | ||
Full Title: Vitamin D and type 2 diabetes. | ||
Medical condition: Type 2 diabetes mellitus and vitamin D insufficiency/deficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002807-21 | Sponsor Protocol Number: VitaD-1 | Start Date*: 2008-10-15 | ||||||||||||||||
Sponsor Name:MUW, Universitätsklinik für Innere Medizin III, Abteilung für Nephrologie und Dialyse | ||||||||||||||||||
Full Title: VITA-D: Cholecalciferol substitution in vitamin D deficient kidney transplant recipients: A randomized, placebo-controlled study to evaluate the posttransplant outcome | ||||||||||||||||||
Medical condition: Vitamin D deficiency in kidney transplant recipients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002113-21 | Sponsor Protocol Number: 0822-009 | Start Date*: 2005-11-09 | |||||||||||
Sponsor Name:Merck & Co. Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter 16 Week Study to Assess the Effect of Vitamin D3 8400 IU Once Weekly on Body Sway and Neuromuscular Function in Men and Women Over 70 Yea... | |||||||||||||
Medical condition: Vitamin D deficiency, unspecified | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024213-31 | Sponsor Protocol Number: UNOLE0166 | Start Date*: 2012-09-12 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: Can Vitamin D Replacement Reduce Insulin resistance In South Asians with Vitamin D Deficiency? | |||||||||||||
Medical condition: Vitamin D Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003755-29 | Sponsor Protocol Number: D-CURE-IV-16-1 | Start Date*: 2016-10-28 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A | |||||||||||||
Full Title: A phase IV, randomised, parallel study to compare a monthly administration of vitamin D3 (D-CURE®) to a daily administration of vitamin D3 (VISTA-D3®). | |||||||||||||
Medical condition: Vitamin D deficiency (10-20 ng/ml) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003417-34 | Sponsor Protocol Number: D-CURE-IV-12-1 | Start Date*: 2012-09-26 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A. | |||||||||||||
Full Title: A phase IV, two-armed, randomised, cross-over study to compare the compliance of a once-a-month administration of vitamin D3 (D-CURE®) to a daily administration of a fixed-dose combination of vitam... | |||||||||||||
Medical condition: Patients are over 50 years old and do not present any significant medical conditions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000508-40 | Sponsor Protocol Number: PAT17-LOADS | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:Pharma Patent Kft. | |||||||||||||
Full Title: Controlled randomized open label clinical study to compare the efficacy and the safety of the loading dose schedules of Vitamin D3 (colecalciferol) 30,000 IU product in deficient patients | |||||||||||||
Medical condition: Vitamin-D deficient patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003673-18 | Sponsor Protocol Number: 1062016 | Start Date*: Information not available in EudraCT |
Sponsor Name:UZ Brussel | ||
Full Title: Can we with vitamin D3, improve the innate immune system? | ||
Medical condition: Immunological problems such as hypogammaglobulinemia with clinical recurrent infections such as sinusitis , pneumonia , otitis , skin infections and gastrointestinal infections. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003779-48 | Sponsor Protocol Number: D-CURE-IV-14-1 | Start Date*: 2014-10-13 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A. | |||||||||||||
Full Title: A phase IV, randomised, cross-over study to estimate the influence of food on the 25-hydroxyvitamin D3 serum level after vitamin D3 (D-CURE®) supplementation. | |||||||||||||
Medical condition: Vitamin D deficiency (10-20 ng/ml) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005232-29 | Sponsor Protocol Number: PAT12-730DS | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:Pharma Patent Kft | |||||||||||||
Full Title: Controlled, randomized, four-arm comparative, open label, multi-centric trial to compare the efficacy and safety parameters of the once-a-week or once-a-month administered 7000 IU, or 30000 IU vita... | |||||||||||||
Medical condition: Vitamin D deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002766-73 | Sponsor Protocol Number: PHT/2014/44 | Start Date*: 2015-10-26 | ||||||||||||||||
Sponsor Name:Portsmouth Hospitals NHS Trust | ||||||||||||||||||
Full Title: The effect of oral Vitamin D supplementation on endothelial function, vascular inflammation, oxidative stress and insulin sensitivity in patients with impaired fasting glucose: A randomised, double... | ||||||||||||||||||
Medical condition: Impaired fasting glycaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022454-17 | Sponsor Protocol Number: 20100812 | Start Date*: 2010-09-29 | |||||||||||
Sponsor Name:University of Liège- Dpt de Médecine Générale | |||||||||||||
Full Title: A double-blind, placebo controlled, randomized, comparative, mono-centre trial to assess the impact of a monthly administration of 50.000 IU of Vitamin D during 6 months on Vitamin D level in he... | |||||||||||||
Medical condition: Vitamine D deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004621-26 | Sponsor Protocol Number: Devitahep | Start Date*: 2012-07-31 | |||||||||||||||||||||
Sponsor Name:Medical University Graz | |||||||||||||||||||||||
Full Title: The effect of vitamin D supplementation on immune response following hepatitis B vaccine in incident and prevalent hemodialysis patients with vitamin D deficiency | |||||||||||||||||||||||
Medical condition: The effect of vitamin D supplementation on immune response following hepatitis B vaccine in incident and prevalent hemodialysis patients with vitamin D deficiency | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005763-24 | Sponsor Protocol Number: CTSUBEST-D | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: BEST-D (Biochemical efficacy and safety trial of vitamin D): a dose-finding trial assessing biochemical and vascular effects of high dose vitamin D | |||||||||||||
Medical condition: BEST-D is a trial assessing the efficacy and safety of vitamin D3 supplements (two doses 50μg and 100μg); hence there are no specific medical conditions under study. Volunteers aged 65 years or old... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001826-84 | Sponsor Protocol Number: DVITEPI01 | Start Date*: 2012-12-13 |
Sponsor Name:University of Pécs | ||
Full Title: The Effect of Vitamin D on the Frequency of Epileptic Seizures: A Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial | ||
Medical condition: Epilepsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
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