- 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 3 of 70.
EudraCT Number: 2015-003108-22 | Sponsor Protocol Number: PAR-C14-007 | Start Date*: 2015-12-08 |
Sponsor Name:NPS Pharmaceuticals, Inc. | ||
Full Title: An Open-label, Single-dose Study to Determine the Pharmacokinetic/Pharmacodynamic Profile of Parathyroid Hormone (rDNA) Administered Subcutaneously at a Dose of 50 µg in Subjects with Hypoparathyr... | ||
Medical condition: Chronic hypoparathyroidism | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002041-12 | Sponsor Protocol Number: SMF 1437 | Start Date*: 2004-11-01 |
Sponsor Name:Gambro Lundia AB, Corporate Research | ||
Full Title: Is it possible to increase free sodium removal by the use of low sodium peritoneal dialysis solution? | ||
Medical condition: Subjects with renal failure treated with peritoneal dialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001807-22 | Sponsor Protocol Number: 9676 | Start Date*: Information not available in EudraCT |
Sponsor Name:uh Montpellier | ||
Full Title: Modalities of vitamin D supplementation and the risk of hypercalcemia in children aged 2 to 6 years | ||
Medical condition: children receiving supplementation | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000931-18 | Sponsor Protocol Number: EL-THOS-001 | Start Date*: 2014-05-27 |
Sponsor Name:Ersi Voskaridou-Dimoula | ||
Full Title: EVALUATION OF EFFICACY OF DENOSUMAB IN PATIENTS WITH THALASSEMIA MAJOR AND OSTEOPOROSIS: A RANDOMIZED, PLACEBO-CONTROLLED, SINGLE-SITE, DOUBLE BLIND PHASE 2B CLINICAL TRIAL | ||
Medical condition: Adult patients with Thalassemia major and osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017999-25 | Sponsor Protocol Number: 20090005 | Start Date*: 2010-11-12 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-Label, Single-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Cinacalcet HCl in Pediatric Subjects Aged 28 Days to < 6 Years with Chronic Kidney Di... | |||||||||||||
Medical condition: Secondary hyperparathyroidism (HPT) in subjects with chronic kidney disease (CKD) receiving maintenance hemodialysis. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003489-28 | Sponsor Protocol Number: VITDCUT | Start Date*: 2018-02-19 |
Sponsor Name:Medizinische Universität Graz | ||
Full Title: Influence of high dose vitamin D3 intake on outcome in pancreatic cancer surgery: prospective, randomized, open, controlled study | ||
Medical condition: vitamin D deficiency - pancreatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-022763-35 | Sponsor Protocol Number: VITAMINDHeartFailure1.0 | Start Date*: 2011-03-31 |
Sponsor Name:Medical University of Graz | ||
Full Title: Vitamin D supplementation in chronic heart failure: a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Chronic stable heart failure (NYHA II-IV, ejection fraction ≤ 40%) Vitamin D deficiency (defined as 25 (OH) Vitamin D ≤ 30ng/ml) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2019-004315-31 | Sponsor Protocol Number: CaEP-B | Start Date*: 2020-04-20 | |||||||||||
Sponsor Name:Julie Gehl | |||||||||||||
Full Title: PHASE II INVESTIGATION OF THE HISTOPATHOLOGIC EFFECT OF CALCIUM ELECTROPORATION ON CANCER IN THE SKIN | |||||||||||||
Medical condition: Cutaneous metastases from solid cancer of any histology | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002024-89 | Sponsor Protocol Number: 3475-177 | Start Date*: 2015-12-23 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | ||
Full Title: A Phase III Study of Pembrolizumab (MK-3475) vs. Chemotherapy in Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Carcinoma (KEYNOTE-177) | ||
Medical condition: Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) DE (Completed) FI (Completed) SE (Completed) IE (Completed) DK (Completed) NL (Completed) FR (Completed) IT (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003380-26 | Sponsor Protocol Number: TCP-304 | Start Date*: 2021-01-05 | |||||||||||
Sponsor Name:Ascendis Pharma Bone Diseases A/S | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial, with an Open-Label Extension, Investigating the Safety, Tolerability and Efficacy of TransCon PTH Admini... | |||||||||||||
Medical condition: Hypoparathyroidism in Adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NO (Completed) FR (Completed) DE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002340-23 | Sponsor Protocol Number: MEIN/19/ZoNe-HYP/001 | Start Date*: 2021-04-20 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
Full Title: Open-label, multicenter, multinational, interventional clinical trial to assess effectiveness and safety of the extemporaneous combination of nebivolol and zofenopril calcium in grade 1 to 2 hypert... | |||||||||||||
Medical condition: Grade 1 and 2 hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002471-27 | Sponsor Protocol Number: 2008-15 | Start Date*: 2008-07-22 |
Sponsor Name:Assistance Publique Hopitaux de marseille | ||
Full Title: Traitement de la Progéria de Hutchinson-Gilford par l’association de pravastatine (Vasten®) et d’acide zolédronique (Zométa®) | ||
Medical condition: Progéria de Hutchinson-Gilford et syndromes progéroides | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018553-35 | Sponsor Protocol Number: SMF1482 | Start Date*: 2010-05-03 | |||||||||||
Sponsor Name:Gambro Lundia AB | |||||||||||||
Full Title: SMARTCIT - A NOVEL CITRATE BASED ANTICOAGULATION | |||||||||||||
Medical condition: Acute renal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2020-004624-41 | Sponsor Protocol Number: 24092020 | Start Date*: 2021-07-07 | ||||||||||||||||
Sponsor Name:Zealand University Hospital | ||||||||||||||||||
Full Title: Calcium Electroporation for Malignant GI Bleeding – a randomized controlled trial | ||||||||||||||||||
Medical condition: Malignant gastrointestinal bleeding | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001519-10 | Sponsor Protocol Number: ALN-GO1-008 | Start Date*: 2022-04-25 | |||||||||||
Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, Pharmacodynamics, and Pharmacokinetics of Lumasiran in Patients with Recurrent Calcium Oxalate Kidney Stone Di... | |||||||||||||
Medical condition: Recurrent calcium oxalate kidney stone disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003158-15 | Sponsor Protocol Number: GA1406 | Start Date*: 2014-10-10 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Limited | ||
Full Title: A randomised, assessor blind, placebo controlled exploratory study in healthy volunteers, to characterise the acid neutralisation activity of sodium alginate oral suspension in the fasted state, us... | ||
Medical condition: To pilot the use of a custom designed pH catheter for the measurement of intragastric pH to characterise the antacid action of Gaviscon Double Action versus placebo. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (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 |
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