- Trials with a EudraCT protocol (537)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
537 result(s) found for: Vitamin D.
Displaying page 1 of 27.
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: 2022-002330-13 | Sponsor Protocol Number: COAM-CFD-01 | Start Date*: 2022-06-22 | |||||||||||
Sponsor Name:Fakultní nemocnice v Motole | |||||||||||||
Full Title: The randomized, double blind study phase III.b of the Comprehensive assessment of the musculoskeletal health in children with cystic fibrosis – on the search for means of improvement | |||||||||||||
Medical condition: musculoskeletal health in children with cystic fibrosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000593-54 | Sponsor Protocol Number: HLS02/2011 | Start Date*: 2011-09-14 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | ||||||||||||||||||
Full Title: Effect of Vitamin D supplementation in HIV-infected children, adolescents and young adults with hypovitaminosis D. | ||||||||||||||||||
Medical condition: Children and young adults with HIV infection and hypovitaminosis D. | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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: 2010-023510-32 | Sponsor Protocol Number: D-CURE-IV-10-1 | Start Date*: 2010-12-23 | |||||||||||
Sponsor Name:Laboratoires SMB S.A. | |||||||||||||
Full Title: A phase IV, randomised, double-blinded, placebo-controlled, parallel study to estimate the influence of vitamin D (D-CURE®) supplementation on the 25-hydroxyvitamin D serum concentration in patient... | |||||||||||||
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: 2006-002595-17 | Sponsor Protocol Number: CT 06-MEGA-001 | Start Date*: 2006-10-25 | |||||||||||
Sponsor Name:Recip AB | |||||||||||||
Full Title: A randomized, double-blind, parallel-group study evaluating efficacy and safety of MEGA tablets compared to Kalcipos® tablets in adult Subjects | |||||||||||||
Medical condition: Vitamin D deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005658-52 | Sponsor Protocol Number: AOI2012LAURICHESSE | Start Date*: 2013-05-15 | |||||||||||
Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
Full Title: / | |||||||||||||
Medical condition: / | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 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: 2016-002459-38 | Sponsor Protocol Number: VITdAL-PICUPilot | Start Date*: 2017-02-28 | |||||||||||
Sponsor Name:Children's Hospital of Eastern Ontario | |||||||||||||
Full Title: Rapid normalization of Vitamin D in critically ill children: A phase II dose evaluation randomized controlled trial (VITdAL-PICU pilot) | |||||||||||||
Medical condition: Critically ill children with severe vitamin D deficiency | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2012-004917-14 | Sponsor Protocol Number: D-CURE-IV-12-2 | Start Date*: 2012-12-03 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A | |||||||||||||
Full Title: A phase IV, randomised, double-blinded, parallel study to estimate the dose-response of vitamin D (D-CURE®) supplementation on the 25-hydroxyvitamin D serum concentration in patients with vitamin D... | |||||||||||||
Medical condition: Patients of 18 years of age or more with vitamin D deficiency | |||||||||||||
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Population Age: Adults, Elderly | 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: 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: 2013-001267-23 | Sponsor Protocol Number: PAT13300CCD | Start Date*: 2013-06-19 | ||||||||||||||||
Sponsor Name:Pharma Patent Kft | ||||||||||||||||||
Full Title: Open label multicentric study to evalute the safety and efficacy of CitrokalciumD 300 mg/300 NE tablets in patients assessed deficiency for supplementation of calcium and vitamin D. | ||||||||||||||||||
Medical condition: Vitamin D and calcium deficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024182-44 | Sponsor Protocol Number: NL3372110110 | Start Date*: 2011-01-12 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: Pilot study: Leucocyte actIvation and endothelial function after oral fat loading combined with VITamin D | |||||||||||||||||||||||
Medical condition: Endothelial function Leukocyte activation Triglyceride metabolism Skin autofluorescence | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
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: 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: 2010-024460-18 | Sponsor Protocol Number: VIDI2 | Start Date*: 2011-07-20 | |||||||||||
Sponsor Name:Umeå Universitet | |||||||||||||
Full Title: Vitamin-D-deficiency in imigrants. Treatment study | |||||||||||||
Medical condition: D-vitaminbrist, D-vitamin insufficiens och suboptimala D-vitaminnivåer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
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