- Trials with a EudraCT protocol (120)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
120 result(s) found for: Cholecalciferol.
Displaying page 1 of 6.
EudraCT Number: 2015-003910-26 | Sponsor Protocol Number: 01/2015 | Start Date*: 2017-12-11 |
Sponsor Name:Núcleo de Estudos de Hipertensão da Beira Interior | ||
Full Title: Fase II, unicenter, open, randomized trial to evaluate the response of Th17 and T regulatory lymphocytes to 24 weeks supplementation with cholecalciferol in patients with arterial hypertension, obe... | ||
Medical condition: Obesity associated arterial hypertension Metabolic syndrome associated arterial hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PT (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: 2019-003101-97 | Sponsor Protocol Number: FJD-NEFROVITD-19-01 | Start Date*: 2020-02-18 |
Sponsor Name:FUNDACION JIMENEZ DIAZ HEALTH RESEARCH INSTITUTE | ||
Full Title: An unicentric, open, randomized and crossover clinical trial to evaluate vitamin D supplementation effect of colecalciferol versus calcidiol in mineral metabolism in hemodialisis patients. | ||
Medical condition: VITAMIN D DEFICIENCY IN HEMODIALISIS PATIENTS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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: 2008-005581-31 | Sponsor Protocol Number: | Start Date*: 2008-11-03 |
Sponsor Name:Organisation name was not entered | ||
Full Title: Betydning af D-vitamin substitution hos overvægtige personer med lavt plasma D-vitamin niveau. Effekter på inflammatoriske markører samt fedt- og muskelmetabolisme. | ||
Medical condition: Overvægte personer med lavt plasma D-vitamin | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000640-10 | Sponsor Protocol Number: GPR-II-18-1 | Start Date*: 2019-10-10 | ||||||||||||||||
Sponsor Name:LABORATOIRES SMB S.A. | ||||||||||||||||||
Full Title: A phase II, randomised, double-blind, and parallel study to estimate the dose-response of vitamin D supplementation in chronic kidney disease patients with secondary hyperparathyroidism and vitamin... | ||||||||||||||||||
Medical condition: chronic kidney disease, stage 3 with secondary hyperparathyroidism and vitamin D deficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005003-88 | Sponsor Protocol Number: SIM15 | Start Date*: 2016-03-15 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
Full Title: Survival Improvement with Cholecalciferol in Patients on Dialysis – The SIMPLIFIED Registry Trial | |||||||||||||
Medical condition: Kidney Failure (requiring dialysis). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011758-16 | Sponsor Protocol Number: 1.1 | Start Date*: 2009-12-16 |
Sponsor Name:Karolinska University Hospital Huddinge | ||
Full Title: A randomized placebo controlled trial of vitamin D3 supplementation to a vulnerable patientsgroup susceptible to uppertract respiratory infections. | ||
Medical condition: Patients with primary or secondary immunodeficiencies and/or patients who have an increased incidence of airborn infections more than 42 infectionsday /year. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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: 2014-004592-23 | Sponsor Protocol Number: DLIFE | Start Date*: 2015-03-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: Phase IV randomized, double blind, placebo-controlled study: role of hypovitaminosis D in heart failure and possible advantages of cholecalciferol (Vit D) administration | |||||||||||||
Medical condition: HEART FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002217-19 | Sponsor Protocol Number: 232100-0024 | Start Date*: 2012-12-13 |
Sponsor Name:Dept of Surgery [...] | ||
Full Title: Postoperative treatment with Vitamin D for patients with a history of Bariatric Surgery in C and U County. | ||
Medical condition: Hypovitaminosis D after bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
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: 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: 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: 2012-003514-14 | Sponsor Protocol Number: HYPODD01 | Start Date*: 2013-06-12 | ||||||||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI NAPOLI FEDERICO II | ||||||||||||||||||
Full Title: HYPOVITAMINOSIS D AND ORGAN DAMAGE IN PATIENTS WITH HYPERTENSION: EFFECTS OF SUPPLEMENTATION WITH CHOLECALCIFEROL | ||||||||||||||||||
Medical condition: HYPERTENSION AND HYPOVITAMINOSIS D | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002188-24 | Sponsor Protocol Number: 2013-002188-24 | Start Date*: 2014-01-16 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: REDUCTION OF POST-THYROIDECTOMY TRANSIENT HYPOCALCEMIA WITH CHOLECALCIFEROL 200,000 IU OS ADMINISTERED FOR ONE MONTH BEFORE SURGERY | |||||||||||||||||||||||
Medical condition: Background: 30% of patients undergoing surgery for total thyroidectomy in the first 24 hours may experience a transient hypocalcaemia (serum calcium <8 mg / dl). According to recent studies, pre-s... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003907-37 | Sponsor Protocol Number: DON3 | Start Date*: 2020-09-08 | |||||||||||
Sponsor Name:Università Campus Bio-Medico | |||||||||||||
Full Title: The effects of vitamin D on bone, muscle and adipose tissue: a phase IV randomized double-blind study. | |||||||||||||
Medical condition: Obese elderly patients with vitamin D deficiency who have scheduled either hip replacement due to osteoarthritis or bariatric surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002387-33 | Sponsor Protocol Number: VitalD | Start Date*: 2008-06-03 | |||||||||||
Sponsor Name:Hôpital Erasme | |||||||||||||
Full Title: Impact of 25-hydroxy vitamin D deficiency and its correction on mineral and bone disorde among hemodialysis patients | |||||||||||||
Medical condition: 25-OH vitamin D deficiency and mineral - bone disorder in hemodialysis patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2017-005050-11 | Sponsor Protocol Number: SeMMIviD | Start Date*: 2019-03-08 | |||||||||||
Sponsor Name:A.O. OSPEDALE DI CIRCOLO E FONDAZIONE MACCHI | |||||||||||||
Full Title: Effects of Selenium and cholecalciferol on hyperthyroidism due to Graves' disease treated with methimazole: a randomized, clinical, open label, pilot trial | |||||||||||||
Medical condition: Graves' disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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