- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Cholecalciferol and calcium.
Displaying page 1 of 3.
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: 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: 2019-003101-97 | 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: 2011-001726-14 | Sponsor Protocol Number: 1/2011 | Start Date*: 2011-12-15 | ||||||||||||||||
Sponsor Name:AUSL DI MODENA | ||||||||||||||||||
Full Title: Supplementetion with vitamin D in patients with chronic heart failure and hypovitaminosis D | ||||||||||||||||||
Medical condition: CHRONIC HEART FAILURE (NYHA CLASS II-III) VITAMIN D DEFICIT | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000526-64 | Sponsor Protocol Number: CHRD2115 | Start Date*: 2020-12-11 | ||||||||||||||||
Sponsor Name:Hospital Center René Dubos | ||||||||||||||||||
Full Title: Study of total post-thyroidectomy hypocalcemia after preoperative cholecalciferol supplementation | ||||||||||||||||||
Medical condition: Thyroidectomy is a common operation. Transient postoperative hypocalcemia is the main complication, resulting in clinical discomfort for patients, longer hospital stays and increased perioperative ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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: 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 (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2010-024588-42 | 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: 2008-000606-36 | Sponsor Protocol Number: 84421383 | Start Date*: 2008-04-07 | |||||||||||
Sponsor Name:Aarhus University Hospital, Dept of Endocrinology and Metabolism C | |||||||||||||
Full Title: Treatment of hypoparathyroidism with subcutaneous PTH (1-84) injections: effects on muscle function and quality of life | |||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018139-98 | Sponsor Protocol Number: HUS-S-D-II | Start Date*: 2010-02-04 |
Sponsor Name:Ville-Valtteri Välimäki | ||
Full Title: Satunnaistettu, sokkoutettu, lumekontrolloitu tutkimus D-vitamiinin suurannoshoidosta – 100 000 tai 200 000 yksikköä D3-vitamiinia suun kautta kolmen kuukauden välein | ||
Medical condition: Tutkittavat ovat terveitä. Tutkimuksessa tutkitaan D3-vitamiinihoidon vastetta tutkittavien seerumin 25OHD tasoissa sekä hoidon turvallisuutta. | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003691-19 | Sponsor Protocol Number: 2007-003691-19 | Start Date*: 2008-01-25 | |||||||||||
Sponsor Name:Dept of Molecular Medicin and Surgery | |||||||||||||
Full Title: Tillskott av vitamin D efter framgångsrik operation för primär hyperparatyreoidism (pHPT) - prospektiv randomiserad dubbelblind studie | |||||||||||||
Medical condition: Effekt av D-vitaminsubstitution efter framgångsrik operation för primär hyperparatyreoidism (pHPT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (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: 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: 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 (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000268-14 | Sponsor Protocol Number: 170113 | Start Date*: 2017-05-15 |
Sponsor Name:ASIH Stockholm Södra, Långbro Park | ||
Full Title: Vitamin D supplementation to palliative cancer patients - A double blind, randomised controlled trial | ||
Medical condition: Any type of incurable cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-006163-22 | Sponsor Protocol Number: PK-VIT-D | Start Date*: 2012-04-20 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Study to evaluate the pharmacokinetic of vitamin D (cholecalciferol) in patients with obesity after bariatric surgery in vitamin D deficiency and after normalization | |||||||||||||
Medical condition: Obese patients after bariatric surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018798-39 | Sponsor Protocol Number: 19022010 | Start Date*: 2010-05-03 |
Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Abteilung für Endokrinologie | ||
Full Title: Correction of vitamin D deficiency in critically ill patients: a randomized, doulbe-blind, placebo-controlled trial | ||
Medical condition: Critically ill patients with vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004028-31 | Sponsor Protocol Number: HIDR-0217/OST | Start Date*: 2017-12-22 | |||||||||||
Sponsor Name:FAES FARMA S.A | |||||||||||||
Full Title: Effect of the administration of different Hidroferol® Soft Gelatine Capsules (calcifediol) and cholecalciferol (Dibase®) regimens on 25(OH)D levels and markers of bone remodelling in postmenopausal... | |||||||||||||
Medical condition: Postmenopausal women with 25 (OH) D deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002586-38 | Sponsor Protocol Number: RPH-1101 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Renapharma AB | |||||||||||||
Full Title: A 12-week clinical double-blind, randomised study of cholecalciferol versus placebo in patients with chronic kidney disease stage 3-4 (CHICK). | |||||||||||||
Medical condition: Chronic renal failure, stage 3-4 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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