- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
41 result(s) found for: Sodium citrate.
Displaying page 1 of 3.
EudraCT Number: 2012-000298-22 | Sponsor Protocol Number: PRENECAL | Start Date*: 2012-12-05 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Study to assess the efficacy and safety of oral potassium citrate on the Prevention of nephrocalcinosis in extreme premature: a clinical trial, randomized, double-blind placebo controlled trial. St... | |||||||||||||
Medical condition: incidence of nephrocalcinosis in extremely preterm infants | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000587-10 | Sponsor Protocol Number: PRECOL2011-1 | Start Date*: 2011-05-04 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: SODIUM PICOSULPHATE AND MAGNESIUM CITRATE VERSUS POLYETHYLENE GLYCOLE (PEG) AS EVACUATING TREATMENT PRIOR TO COLONOSCOPY: PHASE IV RANDOMIZED TRIAL | |||||||||||||
Medical condition: � Subjects who are candidate to undergo colonoscopy: � Diagnosis � Screening � Follow-up after previous polipectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002068-42 | Sponsor Protocol Number: B14CS | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Advicenne | |||||||||||||
Full Title: Open label, multicentre study, evaluating the safety, tolerability, efficacy, compliance and the acceptability of alkalising treatments at long-term in patients with cystinuria | |||||||||||||
Medical condition: Cystinuria | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002562-12 | Sponsor Protocol Number: ENDOS2019 | Start Date*: 2019-09-09 |
Sponsor Name:HOSPITAL GENERAL DE CATALUNYA | ||
Full Title: PRAGMATIC, COMPARATIVE AND RANDOMIZED CLINICAL TRIAL OF THE NEW SOLUTION OF 1 LITER POLYETHYLENE GLYCOL VERSUS SODIUM PICOSULFATE WITH MAGNESIUM CITRATE IN THE EFFECTIVENESS OF SCREENING AND SURVE... | ||
Medical condition: Screening and surveillance colonoscopy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001321-17 | Sponsor Protocol Number: 11275 | Start Date*: 2016-12-02 | ||||||||||||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||||||||||||
Full Title: A randomised control trial of 5-Aminolevulinic Acid in combination with Sodium Ferrous Citrate to Enhance Cardioprotection in Adults undergoing Cardiac Surgery | ||||||||||||||||||||||||||||
Medical condition: Low cardiac output states following cardioplegic arrest for cardiac surgery | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: View results |
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: 2020-001135-27 | Sponsor Protocol Number: 000000 | Start Date*: 2020-09-11 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Oxford / Clinical Trials and Research Governance | |||||||||||||||||||||||||||||||||
Full Title: Pre-operative 5-Aminolevulinic acid to activate haem oxygenase to improve outcomes in cardiac surgery: A dose finding study | |||||||||||||||||||||||||||||||||
Medical condition: Cardioprotection for coronary artery bypass graft surgery | |||||||||||||||||||||||||||||||||
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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: 2015-002004-92 | Sponsor Protocol Number: OralRehyd | Start Date*: 2015-09-09 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Klinische Abteilung für allgemeine Pädiatrie | |||||||||||||
Full Title: Acute gastroenteritis in paediatrics : Comparison of two oral rehydration preparations - A randomized pilot study | |||||||||||||
Medical condition: acute gastroenteritis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004944-39 | Sponsor Protocol Number: NPJ005-DM2-0522 | Start Date*: 2018-04-27 | |||||||||||
Sponsor Name:neopharma Japan Co., Ltd | |||||||||||||
Full Title: A 24 Week, Phase IIa, Double blind, Randomized, Parallel Group, Placebo-controlled, Proof of Concept Study to Assess the Efficacy and Safety of Two Doses of 5 Aminolevulinic Acid Co-administered wi... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) HU (Completed) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002364-25 | Sponsor Protocol Number: NOR-01/2011(PDR) | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:Norgine Limited | |||||||||||||
Full Title: A multi-centre, randomised, investigator-blinded study comparing the polyp detection rate of two different types of bowel preparation: a 2-litre solution (MOVIPREP®) versus a hyperosmotic and stimu... | |||||||||||||
Medical condition: Patients with clinical symptoms or polyp history scheduled for either a diagnostic/surveillance colonoscopy or for a screening procedure in patients with a personal or familial risk of colon neopla... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004361-12 | Sponsor Protocol Number: FER-CIT-2016-01 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Fernando Sánchez | ||||||||||||||||||
Full Title: Oxidative stress and extracellular nucleosomes in critically ill patients with acute kidney failure treated with continuous renal replacement therapies. Effect of two anticoagulation strategies of ... | ||||||||||||||||||
Medical condition: Acute renal failure (ARF). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019317-22 | Sponsor Protocol Number: PMF104BC1/10 | Start Date*: 2010-07-02 | |||||||||||
Sponsor Name:PROMEFARM | |||||||||||||
Full Title: Efficacy and tolerability of a new reduced volume bowel preparation before colonoscopy. A multi-centre, randomised, observer-blind, comparative trial vs PEG + Ascorbate. | |||||||||||||
Medical condition: Medical conditions requiring the complete emptying of large intestin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002772-12 | Sponsor Protocol Number: 2020PI088 | Start Date*: 2020-07-17 | |||||||||||
Sponsor Name:CHRU NANCY | |||||||||||||
Full Title: Efficacy of infusions of mesenchymal stem cells from Wharton jelly in the moderate to severe SARS-Cov-2 related acute respiratory distress syndrome (COVID-19): A Phase IIa double-blind randomized ... | |||||||||||||
Medical condition: Moderate to severe SARS-Cov-2 related acute respiratory distress syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001262-15 | Sponsor Protocol Number: BiPhox-Trial | Start Date*: 2020-03-02 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: Comparison of Biphozyl® and Phoxilium® as a replacement fluid during Continuous Veno-Venous Hemofiltration (CVVH) with Regional Citrate Anticoagulation (RCA) for Acute Kidney Injury (AKI) in adults... | ||
Medical condition: Acute Kidney Injury (AKI). This is a A prospective, randomized, controlled, open, cross-over, Phase II, single-center pilot study to assess the effects of two different continuous veno-venous hemof... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003278-15 | Sponsor Protocol Number: AGO/2017/005 | Start Date*: 2017-12-14 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Hyperalgesia, Persistent Pain, and Fentanyl Dosing in On-Pump Coronary Artery Bypass Grafting | ||
Medical condition: Secondary wound hyperalgesia Persistent Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003140-71 | Sponsor Protocol Number: RMFPC-22 | Start Date*: 2020-08-25 | |||||||||||
Sponsor Name:Rockwell Medical, Inc. | |||||||||||||
Full Title: Hemoglobin maintenance in pediatric ESRD patients by ferric pyrophosphate citrate (FPC) | |||||||||||||
Medical condition: Iron deficiency anaemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004959-23 | Sponsor Protocol Number: NPJ005-DM2-0521 | Start Date*: 2018-07-05 | |||||||||||
Sponsor Name:neopharma Japan Co., Ltd | |||||||||||||
Full Title: A 24-week, Phase IIa, Double blind, Randomized, Parallel Group, Placebo controlled, Exploratory Study to Evaluate the Efficacy and Safety of 5 Aminolevulinic Acid Co-administered with Sodium Ferrou... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus in Patients who have not Achieved Adequate Glycemic Control with Maximum Tolerated Dose of Metformin Daily or Sulfonylurea | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002053-31 | Sponsor Protocol Number: ALEC4005 | Start Date*: 2005-08-16 |
Sponsor Name:Hammersmith Hospital | ||
Full Title: To determine the diagnostic accuracy of MRI in detecting lymph node metastases using USPIO (Ultra small super-paramagnetic iron oxide particles) in patients with gynecological malignancy | ||
Medical condition: Gynaecological malignancies | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-001838-29 | Sponsor Protocol Number: TEATE | Start Date*: 2015-01-08 | ||||||||||||||||
Sponsor Name:"G. d'Annunzio" University | ||||||||||||||||||
Full Title: PrevenTion of contrast‐inducEd nephroAThy with urinE alkalinization: the TEATE study | ||||||||||||||||||
Medical condition: contrast‐induced nephroathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002969-27 | Sponsor Protocol Number: PMF104PD1-2-3/2013 | Start Date*: 2015-12-11 | |||||||||||
Sponsor Name:Alfa Wassermann S.p.A. | |||||||||||||
Full Title: A RANDOMISED, SINGLE-BLIND, ACTIVE CONTROLLED, MULTI-CENTRE TRIAL TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, ACCEPTABILITY AND PALATABILITY OF PMF104 COMPARED TO A CONVENTIONAL PEG-ELECTROLYTE... | |||||||||||||
Medical condition: Need of bowel cleansing in order to perform a colonoscopy or any other diagnostic or therapeutic procedure concerning the colon. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) BE (Completed) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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