- Trials with a EudraCT protocol (1,385)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,385 result(s) found for: Calcium.
Displaying page 4 of 70.
EudraCT Number: 2020-001071-33 | Sponsor Protocol Number: Birr20201 | Start Date*: 2022-02-03 |
Sponsor Name:BirrBeheerBV | ||
Full Title: Role of the intestine on osteoarthritis of the hand and the effect of Sustained Release Calcium Butyrate. | ||
Medical condition: Osteoarthritis of the hand | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004987-91 | Sponsor Protocol Number: 2020/ABM/01/00098 | Start Date*: 2021-11-17 | |||||||||||
Sponsor Name:Uniwersytet Medyczny im. Piastów Śląskich we Wrocławiu | |||||||||||||
Full Title: Effects of calcium electroporation, electrochemotherapy, and irreversible electroporation (IRE-CaCl2, ECT and IRE) on quality of life and progression – free survival in patients with pancreatic can... | |||||||||||||
Medical condition: Unresectable pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000538-21 | Sponsor Protocol Number: PRP-GTPS-2019 | Start Date*: 2019-09-12 |
Sponsor Name:ISABEL ANDIA ORTIZ | ||
Full Title: PAINFUL SYNDROME OF THE MAJOR TROCANTER: Randomized clinical trial with masked evaluation of parallel groups to evaluate the efficacy and safety of the sub-fascial infiltration of PRP compared with... | ||
Medical condition: Painful syndrome of the greater trochanter (chronic GTPS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017649-67 | Sponsor Protocol Number: nnisbjl2009 | Start Date*: 2010-06-22 |
Sponsor Name:The Central Remedial Clinic and The Children's University Hospital | ||
Full Title: Bone Health in Duchenne Muscular Dystrophy- a case controlled study of Risedronate use | ||
Medical condition: Bone Health in Duchenne Muscular Dystrophy- a randomised controlled study of Risedronate use | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011378-14 | Sponsor Protocol Number: M10-967 | Start Date*: 2009-11-03 | ||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | ||||||||||||||||||
Full Title: The IMPACT SHPT Study: Study to Evaluate the Improved Management of iPTH with Paricalcitol-centered Therapy vs. Cinacalcet Therapy with Low-dose Vitamin D in Hemodialysis Patients with Secondary H... | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism (SHPT) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) NL (Completed) ES (Completed) PT (Completed) GB (Completed) SE (Completed) IT (Completed) GR (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006210-14 | Sponsor Protocol Number: 20080579 | Start Date*: 2009-04-30 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: Phase 2 Open-Label Single-Arm, Multi-Center Study to Evaluate the Safety and Efficacy of Sunitinib Malate in Combination with AMG 386 as First Line or Second Line Therapy for Subjects with Metastat... | |||||||||||||
Medical condition: Metastatic renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002981-29 | Sponsor Protocol Number: RC-P0050 | Start Date*: 2017-09-12 | |||||||||||
Sponsor Name:Groupement des Hôpitaux de l’Institut Catholique de Lille | |||||||||||||
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: 2015-001761-11 | Sponsor Protocol Number: 300488 | Start Date*: 2015-08-31 | ||||||||||||||||
Sponsor Name:The Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital | ||||||||||||||||||
Full Title: Lymphatic dysfunction as a cause of calcium channel blocker oedema in post-menopausal women | ||||||||||||||||||
Medical condition: Calcium channel antagonist induced peripheral edema in post-menopausal women. We hypothesize that this condition is partly due to impaired lymphatic function in these patients. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005752-10 | Sponsor Protocol Number: 956 | Start Date*: 2016-03-11 | |||||||||||
Sponsor Name:University Hospitals of North Midlands NHS Trust | |||||||||||||
Full Title: The relationship between computerised tomographic coronary angiography (CTCA) calcium scoring and endothelial progenitor cell (EPC) count. Study A and B. | |||||||||||||
Medical condition: Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003011-97 | Sponsor Protocol Number: 69HCL20_0071 | Start Date*: 2020-12-14 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Fluconazole as a new therapeutic tool in hypercalciuric patients with increased 1,25(OH)2D levels. | |||||||||||||
Medical condition: Hypercalciuria | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2008-006413-25 | Sponsor Protocol Number: GA0821 | Start Date*: 2008-12-09 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Limited | ||
Full Title: A single-centre randomised, partially blind, single dose, crossover study investigating the onset of action of soothing and cooling after taking Gaviscon Peppermint liquid, Double Action Gaviscon ... | ||
Medical condition: Symptoms of heartburn | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000839-33 | Sponsor Protocol Number: LP0053-1108 | Start Date*: 2016-03-23 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Safety and Effect of LEO 90100 aerosol foam on the HPA Axis and Calcium Metabolism in Adolescent Subjects (Aged 12 to < 17 Years) with Plaque Psoriasis A phase 2 trial evaluating the safety and e... | |||||||||||||
Medical condition: Plague Psoriasis | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005434-12 | Sponsor Protocol Number: Nephropaed-PD-01/B | Start Date*: 2008-07-02 | ||||||||||||||||
Sponsor Name:Universitaetsklinikum Erlangen | ||||||||||||||||||
Full Title: Randomized, multicenter cross-over study investigating the effect of bicarbonate-based solutions (Physioneal 35 vs. 40) on protein metabolism in children and adolescents on chronic peritoneal dialysis | ||||||||||||||||||
Medical condition: Pediatric and adolescent patients with end-stage renal failure undergoing chronic peritoneal dialysis | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-009427-11 | Sponsor Protocol Number: PD-NL-04-EU | Start Date*: 2010-10-13 | |||||||||||
Sponsor Name:Fresenius Medical Care Deutschland GmbH | |||||||||||||
Full Title: Efecto de la solución de diálisis peritoneal balance sobre la membrana peritoneal de pacientes tratados con diálisis peritoneal automatizada (DPA) (The effect of balance peritoneal dialysis solutio... | |||||||||||||
Medical condition: Pacientes con enfermedad renal crónica tratados con diálisis peritoneal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002653-31 | Sponsor Protocol Number: VF20040171 | Start Date*: 2004-11-25 |
Sponsor Name:Odense University hospital | ||
Full Title: CAPHI. Profylactic effect of Ca2+ sensitizer versus phosphodiesterase inhibitor infusion at CAGB patients with preoperative low ejection fraction. A prospective randomised clinical trial. | ||
Medical condition: Perioperative use of Milrinon to CAGB patients has shown to reduce postoperative complications. Levosimendan improves cardiac performance without interfering with the calcium turnover and there by ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001198-18 | Sponsor Protocol Number: ITS2006-1 | Start Date*: 2006-05-30 |
Sponsor Name:Sligo General Hospital | ||
Full Title: Improving Tolerability of Statins | ||
Medical condition: Subjects for whom statin intake is a necessary therapeutic intervention i.e diabetics, dyslipidemics and patients with ischaemic heart disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001394-29 | Sponsor Protocol Number: 31998 | Start Date*: 2007-12-28 | |||||||||||
Sponsor Name:Baxter Healthcare Corporation | |||||||||||||
Full Title: Multi-center, prospective trial to demonstrate Improved Metabolic control of PPEN vs DDDD in DIAbetic CAPD patients -The IMPENDIA Trial | |||||||||||||
Medical condition: End stage renal disease patients with Diabetes Type I and II on Continuous Ambulatory Peritoneal Dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) AT (Completed) IT (Prematurely Ended) CZ (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006246-34 | Sponsor Protocol Number: CL3-16257-068 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the anti-anginal efficacy and safety of oral administration of ivabradine compared to placebo on top of a background therapy with a calcium antagonist (amlodipine or nifedipine) in pa... | |||||||||||||
Medical condition: Stable angina pectoris | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) EE (Completed) HU (Completed) PL (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006130-95 | Sponsor Protocol Number: A2581173 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:PFIZER | |||||||||||||
Full Title: Estudio abierto, prospectivo, de tres años de duración para evaluar la eficacia, la seguridad y la tolerabilidad clínicas de la atorvastatina en niños y adolescentes con hipercolesterolemia famili... | |||||||||||||
Medical condition: "Hipercolesterolemia familiar heterocigótica (HFHe) en niños y adolescentes" "HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA IN CHILDREN AND ADOLESCENTS" | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) BE (Completed) IT (Completed) DE (Completed) GR (Completed) SK (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
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