- Trials with a EudraCT protocol (159)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    159 result(s) found for: Calcium metabolism.
                    
                
			
   			
		
		Displaying page 1 of 8.
	
	
	| 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: 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: 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: 2021-001730-19 | Sponsor Protocol Number: v1-2 | Start Date*: 2022-02-24 | 
| Sponsor Name:Medical Univerity of Vienna | ||
| Full Title: Hormones and Muscle – Unravelling the metabolic pathways of endocrine myopathies A translational magnetic resonance spectroscopy and imaging pilot study | ||
| Medical condition: Hypothyroidism Hypoparathyroidism | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-002221-31 | Sponsor Protocol Number: CCB-CRC-05-1 | Start Date*: 2005-08-11 | 
| Sponsor Name:Clinic for Nephrology | ||
| Full Title: Efficacy of niacin on phosphatic metabolism in patients with renal insufficiency | ||
| Medical condition: Exam the efficacy of niaspan in phosphate metabolism of patients with renal insufficiency, different exam for dialysis and predialysis patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (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: 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: 2008-000606-36 | 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: 2017-002096-26 | Sponsor Protocol Number: MV-3-2017 | Start Date*: 2017-08-24 | ||||||||||||||||||||||||||
| Sponsor Name:Universitetsklinik for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro; Hospitalsenheden Vest | ||||||||||||||||||||||||||||
| Full Title: Investigate the differences between treating Chronic Kidney Disease - Mineral and Bone Disorder with an iron-containing phosphate binder or a calcium-containing phosphate binder in dialysis patients. | ||||||||||||||||||||||||||||
| Medical condition: Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially bone metabolism and blood vessel calcification | ||||||||||||||||||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| 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: 2012-005416-26 | Sponsor Protocol Number: ANSWER | Start Date*: 2014-06-06 | 
| Sponsor Name:Mario Negri Institute | ||
| Full Title: A Prospective, Randomized, Open, Blinded Endpoint (PROBE), Clinical Trial to Assess The Renal and Humoral Effects of Sevelamer Carbonate in Patients with Chronic Kidney Disease and Residual Protein... | ||
| Medical condition: Chronic Kidney Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| 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: 2018-000685-12 | Sponsor Protocol Number: MC2-01-C6 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:MC2 Therapeutics Ltd | |||||||||||||
| Full Title: A Multicentre, Open-label, Single-group Maximal Use Trial, Evaluating the Safety and Pharmacokinetic Profile of the Active Ingredients and their Metabolites after application of MC2-01 Cream in Ado... | |||||||||||||
| Medical condition: Extensive Psoriasis Vulgaris | |||||||||||||
| 
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) CZ (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005303-91 | Sponsor Protocol Number: VIT_D_2015 | Start Date*: 2016-07-04 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE | |||||||||||||
| Full Title: Clinical Trial of pharmacokinetics of calcifediol (25OHD3) in women with postmenopausal osteoporosis | |||||||||||||
| Medical condition: postmenopausal osteoporosis | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001704-23 | Sponsor Protocol Number: PHPT_002/08 | Start Date*: 2009-09-03 | |||||||||||
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Chirurgie | |||||||||||||
| Full Title: Primary hyperparathyroidism: does a systematic treatment improve the calcium and bone metabolism after successful surgery? – Part II Systematic treatment of patients with neither osteopenia nor os... | |||||||||||||
| Medical condition: Hypothesis: Calcium and vitamin D intake after surgery for PHPT protects the bone by keeping PTH in the normal range (less secondary, reactive hyperparathyroidism), prevents hungry bone- syndrome a... | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002270-52 | Sponsor Protocol Number: CIRIVA | Start Date*: 2013-12-05 | |||||||||||
| Sponsor Name:Hospital Universitari de Girona Dr.Josep Trueta | |||||||||||||
| Full Title: Effects of cinacalcet versus conventional treatment on metabolism bone and vascular involvement in advanced chronic renal failure | |||||||||||||
| Medical condition: Bone's disorders and mineral metabolism and vascular involvement | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000573-29 | Sponsor Protocol Number: 20062007 | Start Date*: 2009-10-16 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Using Cinacalcet to Correct Hypercalcemia in Renal Transplant Recipients With Autonomous Hyperparathyroid... | |||||||||||||
| Medical condition: Renal transplant recipients with hypercalcemia and autonomous hyperparathyroidism | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) FR (Completed) ES (Completed) IT (Completed) AT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002095-10 | Sponsor Protocol Number: MV-2-2017 | Start Date*: 2017-09-13 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Universitetsklinik for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro; Hospitalsenheden Vest | ||||||||||||||||||||||||||||||||||||||
| Full Title: Investigate the differences between treating Chronic Kidney Disease - Mineral and Bone Disorder with an iron-containing phosphate binder or a calcium-containing phosphate binder in Chronic Kidney D... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially bone metabolism and blood vessel calcification | ||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-000171-17 | Sponsor Protocol Number: SPD405-207 | Start Date*: 2012-10-02 | |||||||||||
| Sponsor Name:Shire Pharmaceutical Development Ltd. | |||||||||||||
| Full Title: A Three Part Open-Label Study to Assess the Pharmacokinetics of Lanthanum Carbonate, compare the Efficacy, Safety and Tolerability of 8 weeks treatment with Lanthanum Carbonate and Calcium Carbonat... | |||||||||||||
| Medical condition: Treatment of Hyperphosphataemia. | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) PL (Completed) Outside EU/EEA CZ (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000354-22 | Sponsor Protocol Number: A3841029 | Start Date*: 2004-12-06 | 
| Sponsor Name:Pfizer Healthcare Ireland | ||
| Full Title: An International, Multicentre, Open Label Study To Assess The Effectiveness Of Amlodipine –Atorvastatin Combination In Subjects With Hypertension and Dyslipidaemia. (The JEWEL II Study) | ||
| Medical condition: Concurrent hypertension (ICD code 80011/MedDRA: coded under preferred term "vascular system order", code 10020772) and dyslipidaemia (ICD code 89212/MedDRA: coded under preferred term "metabolism a... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Completed) ES (Completed) AT (Completed) HU (Completed) IT (Completed) | ||
| Trial results: View results | ||
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