- Trials with a EudraCT protocol (1,385)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (75)
1,385 result(s) found for: Calcium.
Displaying page 12 of 70.
EudraCT Number: 2012-005040-20 | Sponsor Protocol Number: 2012-520 | Start Date*: 2013-01-09 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of Macrodex versus lactated Ringer on coagulation in major surgery. A randomised clincal trial. | |||||||||||||
Medical condition: Neoplasma malignum vesicae urinaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002913-37 | Sponsor Protocol Number: MPN-001-07-2018 | Start Date*: 2019-03-13 |
Sponsor Name:Antibiotic-Razgrad AD | ||
Full Title: Multicenter, prospective, randomized, double-blind, two-armed phase IV clinical study for efficacy and safety assessment of two 2% mupirocin containing nasal ointments (MupiroNasal 20mg/g, nasal oi... | ||
Medical condition: For elimination/eradication of nasal carriage of staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003855-38 | Sponsor Protocol Number: PIERAID-2013 | Start Date*: 2014-09-26 |
Sponsor Name:Miguel Giovanni Uriol Rivera | ||
Full Title: Benefits of paricalcitol (Selective vitamin D receptor activator indicated for the prevention and treatment of secondary hyperparathyroidism) on anaemia of inflammation in dialysis patients receiv... | ||
Medical condition: Anaemia of inflammation in patients with chronic kidney disease on haemodialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003441-16 | Sponsor Protocol Number: ML20570 | Start Date*: 2006-12-12 | |||||||||||
Sponsor Name:N.V. Roche S.A. | |||||||||||||
Full Title: OPEN LABEL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF INTRAVENOUS LOADING DOSE OF 3X 6MG IBANDRONIC ACID (BONDRONAT®) DURING 3 CONSECUTIVE DAYS IN PATIENTS WITH BREAST CANCER AND SKELETAL METASTA... | |||||||||||||
Medical condition: Metastasic bone pain in patients with breast cancer and bone metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015217-52 | Sponsor Protocol Number: Uni-Koeln-1251 | Start Date*: 2010-06-08 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Pilotstudie zur Pyridoxalphosphattherapie bei Patienten mit primärer Hyperoxalurie Typ I - Pilot trial on treatment of patients with primary hyperoxaluria type I with pyridoxal-phosphate | |||||||||||||
Medical condition: In this study we will prospectively analyze the reduction of urinary oxalate excretion under the treatment with PLP in dosages of 5mg/kg/day up to 20 mg/kg/day and serum level response relationship... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013159-31 | Sponsor Protocol Number: CS/2009/3292 | Start Date*: 2010-02-25 |
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||
Full Title: Preoperative volume replacement vs. usual care in diabetic patients having CABG surgery: a randomised controlled trial | ||
Medical condition: Coronary artery bypass grafting in diabetic patients | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006782-83 | Sponsor Protocol Number: EC08/00230 | Start Date*: 2013-09-24 |
Sponsor Name:Hospital Universitario Virgen de las Nieves | ||
Full Title: Prevention MODS by modulating the inflammatory response through melatonin administration in surgical patients with severe sepsis. | ||
Medical condition: Septic patients of abdominal surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001347-31 | Sponsor Protocol Number: M13-954 | Start Date*: 2013-11-12 |
Sponsor Name:Abbott Laboratories GmbH | ||
Full Title: A Double-blind, Randomized, Multi-center, Placebo-controlled, Parallel-group Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in Subjects with Diabetes Mellitus type 2 | ||
Medical condition: Pancreatic exocrine insufficiency in diabetes type II | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003260-32 | Sponsor Protocol Number: 13090 | Start Date*: 2013-12-04 |
Sponsor Name: | ||
Full Title: The Effects of Isovolumetric and Isoeffective Infusions of Colloid Versus Crystalloid on Renal Blood Flow and Cardiac Output | ||
Medical condition: Anaesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (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: 2005-000117-34 | Sponsor Protocol Number: Nordic VII | Start Date*: 2005-04-22 |
Sponsor Name:The Nordic Colorectal Cancer Biomodulation Group | ||
Full Title: Combination of 5-Fluorouracil/Folinate/Oxaliplatin (Eloxatin®) (FLOX regimen) with Concomitant or Concomitant and Maintenance Administration of Cetuximab (Erbitux®), in First-Line Treatment of Meta... | ||
Medical condition: Patient with metastatic colorectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) IS (Completed) FI (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001152-19 | Sponsor Protocol Number: VitDBR2012 | Start Date*: 2013-02-28 | |||||||||||
Sponsor Name:Antonio Moreno Galdó | |||||||||||||
Full Title: Effect of supplementation with vitamin D on the acute bronchitis prevention during the first year of life. | |||||||||||||
Medical condition: Acute bronchitis Upper airway infection | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011299-32 | Sponsor Protocol Number: 20060359 | Start Date*: 2010-08-06 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Phase 3 Study of Denosumab as Adjuvant Treatment for Women with Early-Stage Breast Cancer at High Risk of Recurrence | |||||||||||||
Medical condition: Early-stage non-metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) GB (Completed) ES (Prematurely Ended) CZ (Completed) LV (Completed) FR (Completed) BE (Completed) SK (Completed) NL (Completed) IE (Prematurely Ended) DK (Completed) SI (Completed) GR (Completed) IT (Completed) BG (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000501-22 | Sponsor Protocol Number: SPON1189-13 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Cardiff Univeristy | |||||||||||||
Full Title: A national cancer research institute acute myeloid leukaemia working group pilot trial under the auspices of the cardiff experimental cancer medicine centre to establish the feasibility of combinin... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002363-15 | Sponsor Protocol Number: EVITA | Start Date*: 2015-02-13 |
Sponsor Name:University Medical Center of the Johannes Gutenberg University Mainz | ||
Full Title: EVITA Trial: Effect of VItamin D as add-on Therapy for vitamin D insufficient patients with severe Asthma: a randomized, double-blind, placebo-controlled trial. | ||
Medical condition: severe asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-002678-11 | Sponsor Protocol Number: ICO-13-001 | Start Date*: 2018-06-07 |
Sponsor Name:Institut Català d’Oncologia | ||
Full Title: An open label biomarker pilot study of the antitumoral acrivity of denosumab in the pre-operative setting of early breast cancer | ||
Medical condition: early breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2019-000274-36 | Sponsor Protocol Number: APACH2 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: Phase III trial comparing 2 diagnostic strategies for the preoperative localization of parathyroid adenoma in primary hyperparathyroidism: TEMP / CT with Tc99m-sestaMIBI or PET / CT with F18-choli... | |||||||||||||
Medical condition: Patient with primary hyperparathyroidism and for which surgical resection is provided. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002026-52 | Sponsor Protocol Number: ACCORD 24/0610 (PRODIGE 24) | Start Date*: 2011-10-11 | |||||||||||
Sponsor Name:Fédération Nationale des Centres de Lutte Contre le Cancer (FNCLCC) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000112-33 | Sponsor Protocol Number: NL47761.041.14 | Start Date*: 2014-09-01 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Apixaban versus antiplatelet drugs or no antithrombotic drugs after anticoagulation-associated intracerebral haemorrhage in patients with atrial fibrillation. A randomised phase II clinical trial. | ||
Medical condition: The prevention of ischaemic stroke in patients with atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000050-22 | Sponsor Protocol Number: SEGCG18-01 | Start Date*: 2018-04-24 | |||||||||||
Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
Full Title: Irinotecan-based triplet (FOLFOXIRI) as perioperative treatment in resectable gastric and gastroesophageal junction adenocarcinoma. | |||||||||||||
Medical condition: Resectabel gastric and gastroesophageal junction adenocarcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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