- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Vitamin B deficiency.
Displaying page 1 of 2.
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: 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: 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: 2010-024129-20 | Sponsor Protocol Number: ProyectoOB12 | Start Date*: 2011-06-07 | |||||||||||
Sponsor Name:Consorcio de Apoyo a la Investigación Biomédica en red (CAIBER) | |||||||||||||
Full Title: Oral Versus Intramuscular Cobalamin to treat Cobalamin Deficiency: Noninferiority randomised controlled trial, pragmatic and multi-center in the primary healthcare setting (OB12 project). | |||||||||||||
Medical condition: Vitamin B12 (cianocobalamin) defficiency | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2016-000503-87 | Sponsor Protocol Number: PAT15-PCODD | Start Date*: 2016-07-13 | |||||||||||
Sponsor Name:Pharma Patent Kft | |||||||||||||
Full Title: A multicentre, Phase III, randomised, double blind, placebo-controlled study to assess the safety and the efficacy of a weekly administered dose of 30,000 IU vitamin D (colecalciferol) in deficien... | |||||||||||||
Medical condition: Vitamin D deficient female subjects diagnosed with PCOS | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2018-001488-21 | Sponsor Protocol Number: EST:15/17 | Start Date*: 2018-11-06 |
Sponsor Name:Sergio Aleman | ||
Full Title: EFFECT OF VITAMIN D SUPPLEMENTATION ON THE VENTRICULAR DEFORMATION RATE (STRAIN RATE) IN PATIENTS WITH HEART FAILURE WITH PRESERVED OR MODERATELY REDUCED EYECTION FRACTION | ||
Medical condition: Heart failure with preserved or moderately reduced eyection fraction | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
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: 2014-003645-10 | Sponsor Protocol Number: 2014-LSB | Start Date*: 2014-11-27 |
Sponsor Name:Department of Endocrinology and Internal Medicine | ||
Full Title: Physiological interactions between the adrenal- and the parathyroid glands described by controlled clinical trials | ||
Medical condition: Secondary hyperparathyrodism due to Vitamin D deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005039-40 | Sponsor Protocol Number: 2006-005039-40HIVD001 | Start Date*: 2007-02-16 | |||||||||||
Sponsor Name:Calcium and Bone Metabolic Unit Copenhange University Hospital Hvidovre | |||||||||||||
Full Title: Vitamin D status hos patienter med HIV infektion - Intervention with vitamin D - a pilot study | |||||||||||||
Medical condition: It has been shown in our clinic that many patients with HIV infektion have vitamin D deficiency and it is the aim to investigate the benefits of correcting this vitamin D deficiency on bone metabol... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2011-002823-16 | Sponsor Protocol Number: 02-2011 | Start Date*: 2011-07-27 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: Effects of Vitamin D in patients affected by heart failure | |||||||||||||
Medical condition: Heart failure is a condition that occurs when the heart loses its normal ability to pump blood to maintain vital body functions and, therefore, works with lower efficiency. Several studies have sho... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004147-37 | Sponsor Protocol Number: 16-047 | Start Date*: 2017-01-31 |
Sponsor Name:Center for Translational & Clinical Research Aachen (CTC-A) | ||
Full Title: Intravenous iron in patients with heart failure and reduced ejection fraction (HFREF) plus iron deficiency: Effects upon phosphate and FGF23 metabolism | ||
Medical condition: Systolic heart failure (heart failure with reduced ejection fraction, HFREF) + iron deficiency with serum ferritin <100 μg/l or 100 – 299 μg/L when transferrin saturation (TSAT) is <20% | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-008692-33 | Sponsor Protocol Number: 2008-242 | Start Date*: 2009-04-21 | ||||||||||||||||
Sponsor Name:Department of Urology, Herlev Hospital | ||||||||||||||||||
Full Title: Evaluation of cytotoxicity and genetic changes of high dose vitamin C infusions in castration resistant metastatic human prostate cancer. | ||||||||||||||||||
Medical condition: The effect of high dose intravenous weekly vitamin c infusion in castration resistant human prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002571-18 | Sponsor Protocol Number: 170KG18 | Start Date*: 2019-07-22 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: EFFECT OF FERRIC CARBOXYMALTOSE ON EXERCISE CAPACITY AFTER KIDNEY TRANSPLANTATION: A MULTICENTER RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Iron deficiency in kidney transplant recipients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005643-26 | Sponsor Protocol Number: PrefoCir2 | Start Date*: 2012-03-15 | ||||||||||||||||
Sponsor Name:ZAMBON ITALIA | ||||||||||||||||||
Full Title: Cross-over pharmacokinetic study and pharmacodynamics of 2 different folate (5-MTHF and folic acid) in patients with liver cirrhosis with viral etiology. A randomized, open-label trial. | ||||||||||||||||||
Medical condition: In all cases of folate deficiency due to increased demand, poor absorption, inadequate dietary intake and reduced utilization of the vitamin in patients with viral liver cirrhosis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000484-13 | Sponsor Protocol Number: AG-348-C-003 | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:Agios Pharmaceuticals Inc | |||||||||||||
Full Title: A Phase 2, Open Label, Randomized, Dose Ranging, Safety, Efficacy, Pharmacokinetic and Pharmacodynamic Study of AG-348 in Adult Patients with Pyruvate Kinase Deficiency | |||||||||||||
Medical condition: Pyruvate Kinase Deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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