- Trials with a EudraCT protocol (1,387)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,387 result(s) found for: Calcium.
Displaying page 8 of 70.
| EudraCT Number: 2017-003660-13 | Sponsor Protocol Number: E-DIS-2-1705 | Start Date*: 2018-02-21 |
| Sponsor Name:Centre Oscar Lambret | ||
| Full Title: Phase II Randomized Study Measuring the Interest of Pursuing or Not the chemotherapy for Non-progressive Patients With Metastatic Esophageal Squamous-cell Cancer After 6 Weeks of LV5FU2-paclitaxel ... | ||
| Medical condition: Patients suffering from squamous-cell type esophageal cancer histologically proved and with metastatic disease measurable according to RECIST criteria. Patients with metachronous metastasis and w... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000411-40 | Sponsor Protocol Number: Version1.0 | Start Date*: 2015-10-23 |
| Sponsor Name:Department of Nuclear Medicine and Endocrinology, Paracelsus Medical University Salzburg | ||
| Full Title: Comparison of the detection of parathyroid adenoms using Tc-99m MIBI scintigraphy and F-18 Choline PET/CT in patients with primary hyperparathyroidism | ||
| Medical condition: Primary hyperparathyroidism due to parathyroid adenoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002329-56 | Sponsor Protocol Number: FISIO | Start Date*: 2021-10-19 | |||||||||||
| Sponsor Name:Sociedad Española de Medicina Intensiva, Crítica y Unidades Coronarias (SEMICYUC) | |||||||||||||
| Full Title: Exploratory study to evaluate the efficacy and safety of nutritionally administering 1.5 g protein/kg/day vs. 1.0 g protein/kg/day in the catabolic phase of the critically ill patient on mechanical... | |||||||||||||
| Medical condition: Acquired Weakness in the Intensive Care Unit (DAUCI) of the critically ill patient. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000028-36 | Sponsor Protocol Number: P3-IMU-838-RMS-01 | Start Date*: 2022-04-21 | |||||||||||
| Sponsor Name:Immunic AG | |||||||||||||
| Full Title: A Multi-Center, Randomized, Double-Blinded Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of IMU-838 versus Placebo in Adults with Relapsing Multiple Sclerosis (ENSURE-1) | |||||||||||||
| Medical condition: Relapsing Multiple Sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Trial now transitioned) BG (Trial now transitioned) GR (Completed) DE (Trial now transitioned) ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001725-25 | Sponsor Protocol Number: RSA-HIP220306 | Start Date*: 2007-08-09 | |||||||||||
| Sponsor Name:GREATER GLASGOW HEALTH BOARD | |||||||||||||
| Full Title: REVISION HP REPLACEMENT - ACETABULAR IMPACTION GRAFTING - A RADIOSTEREOMETRIC COMPARISON BETWEEN FRESH FROZEN ALLOGRAFT AND MARROW-DEPLETED BONE WITH CALCIUM PHOSPHATE PLUS OR MINUS BONE MORPHOGENI... | |||||||||||||
| Medical condition: REVISION HIP REPLACEMENT | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005188-12 | Sponsor Protocol Number: Clinical Protocol | Start Date*: 2005-02-25 |
| Sponsor Name:University of Leeds | ||
| Full Title: DENTAL TRAUMA: The effectiveness of an internet based computer database for data collection in a randomised controlled trail to evaluate immediate extirpation of necrotic pulp tissue and placement ... | ||
| Medical condition: Tooth Avulsion and Replantation | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005746-39 | Sponsor Protocol Number: IH 001 (ACT 2) | Start Date*: 2006-02-21 |
| Sponsor Name:Ineos Healthcare Ltd | ||
| Full Title: A multicentre Phase II study with Alpharen™: an open-label, dose-ranging phase followed by a placebo-controlled, double-blind, parallel-group comparison in haemodialysis subjects with hyperphosphat... | ||
| Medical condition: Hyperphosphataemia in haemodialysis subjects | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000605-12 | Sponsor Protocol Number: notapplicable1 | Start Date*: 2014-06-13 |
| Sponsor Name: | ||
| Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of calcineurin inhibitor-induced hypertension in patients with psoriasis or eczema: a single-center randomized cross-over trial. | ||
| Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004704-35 | Sponsor Protocol Number: NL39417.078.12 | Start Date*: 2012-11-22 |
| Sponsor Name: | ||
| Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of tacrolimus-induced hypertension in dermatology patients: a single-center randomized cross-over trial. | ||
| Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015058-38 | Sponsor Protocol Number: OR09/9018 | Start Date*: 2010-10-22 |
| Sponsor Name:University of Leeds | ||
| Full Title: Improving the outcome for patients after osteoporotic femoral fractures | ||
| Medical condition: OSTEOPOROTIC FEMORAL FRACTURE | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004793-34 | Sponsor Protocol Number: P171103J | Start Date*: 2018-07-10 |
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
| Full Title: 68Ga-DOTATATE PET-CTA imaging for the early detection of progressing coronary atherosclerosis | ||
| Medical condition: Patients with coronary atherosclerosis without significant myocardial ischemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-000693-31 | Sponsor Protocol Number: COLO CP-01 | Start Date*: 2005-06-17 |
| Sponsor Name:Colotech A/S | ||
| Full Title: An international, multi centre, randomised, parallel group, prospective, double blind, placebo controlled clinical trial evaluating the efficacy and safety of a combination treatment administered o... | ||
| Medical condition: Patients who have had removal of polyp in colon or rectum within 3 months. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003354-24 | Sponsor Protocol Number: 2013-NIGRAM-VUMC-001 | Start Date*: 2015-01-08 |
| Sponsor Name:Vrij Universiteit Medical Center | ||
| Full Title: Influence of exogenous growth hormone administration on circulating levels of Klotho in healthy and CKD subjects | ||
| Medical condition: Cardiovascular disease in chronic kidney disease | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001471-36 | Sponsor Protocol Number: PrimeRT-2018 | Start Date*: 2020-10-05 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
| Full Title: Priming the Tumour MicroEnvironment for Effective Treatment with Immunotherapy in Locally Advanced Rectal Cancer: A Phase II trial of Durvulamab in Combination with Extended Neoadjuvant Regimens i... | |||||||||||||
| Medical condition: Rectal Cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2010-018495-25 | Sponsor Protocol Number: EBP-FHC-2010-1 | Start Date*: 2010-05-12 |
| Sponsor Name:Medicinsk Forskning | ||
| Full Title: Effekten af atorvastatin på NO-systemet hos raske kontrol personer | ||
| Medical condition: Effekten af atorvastin på NO-systemet under på raske forsøgspersoner | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006126-10 | Sponsor Protocol Number: Efalizumab in CTCL | Start Date*: 2008-11-27 |
| Sponsor Name:Charité - University Hospital Berlin | ||
| Full Title: pilot study to evaluate the efficacy of Efalizumab in patients with cutaneous t-cell lymphoma | ||
| Medical condition: The cutaneous T-cell lymphoma (also known as Sézary syndrome) is a common disorder of proliferated cells with characteristics of maligne t-lymphocytes immigrating from the cutaneous blood vessels t... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005308-12 | Sponsor Protocol Number: 1111 | Start Date*: 2018-09-07 | |||||||||||
| Sponsor Name:Region Sjælland, Slagelse Hospital | |||||||||||||
| Full Title: Treatment of MRSA throat carriage with mupirocin irrigation | |||||||||||||
| Medical condition: Patientents being MRSA positive for a minimum of 6 months and concluded at least one konventional topical treatments unsuccessfully | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000710-53 | Sponsor Protocol Number: RD.06.SPR.18131 | Start Date*: 2014-12-19 | |||||||||||
| Sponsor Name:GALDERMA R&D, LLC | |||||||||||||
| Full Title: A multicenter open label uncontrolled study of the long term safety and efficacy of calcitriol 3 mcg/g ointment applied twice daily for 26 weeks in pediatric subjects (2 to 16 years and 11 months o... | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) BE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003067-36 | Sponsor Protocol Number: SHP634-404 | Start Date*: 2018-06-28 | |||||||||||||||||||||
| Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||||||||||||
| Full Title: An Open-label Study Investigating the Safety and Efficacy of rhPTH(1-84) in Subjects with Hypoparathyroidism. | |||||||||||||||||||||||
| Medical condition: Hypoparathyroidism | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: HU (Completed) DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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