- Trials with a EudraCT protocol (173)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
173 result(s) found for: Nutritional value.
Displaying page 1 of 9.
EudraCT Number: 2014-002322-12 | Sponsor Protocol Number: Ironsuppletiontrial | Start Date*: 2014-07-24 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Optimizing Iron suppletion trial after Roux- en -Y Gastric Bypass | ||
Medical condition: Patients who underwent a gastric bypass and develop an irondeficiency postoperatively. The medical condition which is investigated is irondeficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000427-20 | Sponsor Protocol Number: NL76691.100.22 | Start Date*: 2022-05-11 |
Sponsor Name:Inreda Diabetic | ||
Full Title: A stable glucagon analog administered by a bihormonal closed loop system; a feasibility study | ||
Medical condition: Type 1 Diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000680-26 | Sponsor Protocol Number: Taurine05 | Start Date*: 2005-06-27 |
Sponsor Name:North west London Hospital Trust | ||
Full Title: A randomised double blind controlled crossover trial of intravenous taurine supplementation in parenteral nutrition as an effective treatment for reducing hepatobiliary complications in chronic int... | ||
Medical condition: Complications of intravenous nutrition include cholestatic liver disease. This is one of the main causes of death during long-term home parenteral nutrition (HPN) and a study in 2000 found that 65%... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004319-33 | Sponsor Protocol Number: D5613C00001 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2b, Randomized, Double blind, Placebo-controlled, Parallel group, Multicentre Dose finding Study to evaluate the Efficacy, Safety and Tolerability of AZD1722 to Treat Hyperphosphatemia in E... | |||||||||||||
Medical condition: Hyperphosphatemia in patients with end-stage renal disease on hemodialysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001972-46 | Sponsor Protocol Number: SKNt-001-CP4 | Start Date*: 2019-05-14 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Reaching Protein Target with SmofKabiven® extra Nitrogen Versus Olimel N9E: A Prospective, Randomised, Active-controlled, Patient-blinded, Multicentre Clinical Trial During the Early Phase of Acute... | |||||||||||||
Medical condition: Parenteral nutrition (PN) when oral or enteral nutrition (ON or EN) is impossible, insufficient, or contraindicated in the early phase of critical illness | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002624-16 | Sponsor Protocol Number: P170907J | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANC-PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Validation of respiratory epithelial functional assessment to predict clinical efficacy of Orkambi®. Pathway to personalized therapy in Cystic Fibrosis PREDICT-CF | |||||||||||||
Medical condition: Homozygous F508del patient aged 12 years or older | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001444-37 | Sponsor Protocol Number: Irontrial | Start Date*: 2014-07-21 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Optimizing iron suppletion after Roux-en-Y Gastric Bypass | ||
Medical condition: Patients who underwent a gastric bypass and develop a irondeficiency postoperatively. The medical condition which is investigated is irondeficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003652-36 | Sponsor Protocol Number: OZR-2011-17 | Start Date*: 2012-11-30 | |||||||||||
Sponsor Name:The Rotterdam Eye Hospital | |||||||||||||
Full Title: The Most Effective Treatment Strategy for Diabetic Macular Edema. | |||||||||||||
Medical condition: diabetic macular edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000976-40 | Sponsor Protocol Number: ION373-CS1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 1-3, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION373 in Patients with Alexand... | |||||||||||||
Medical condition: Alexander Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002963-40 | Sponsor Protocol Number: IDAPADM1 | Start Date*: 2015-10-26 | |||||||||||
Sponsor Name:Dra Cristina Avendaño Sola | |||||||||||||
Full Title: Impact of treatment with Dapagliflozin (SGLT2 inhibitor) in metabolic control and glycemic pattern in type 1 diabetic patients | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003597-17 | Sponsor Protocol Number: FAR-NP-2014-01 | Start Date*: 2014-11-17 | ||||||||||||||||
Sponsor Name:Josep Llop Talaveron | ||||||||||||||||||
Full Title: Pilot, randomized, double-blind clinical trial to determine the phytosterolaemia in hospitalized patients treated with total parenteral nutrition and gamma-glutamyltransferase alteration | ||||||||||||||||||
Medical condition: Adult hospitalized patients with parenteral nutrition and liver disfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002947-32 | Sponsor Protocol Number: 02GPR2021 | Start Date*: 2021-10-28 |
Sponsor Name:Celon Pharma SA | ||
Full Title: A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Evaluate Efficacy, Safety and Pharmacokinetics after 2-weeks Administration of CPL207280 (GPR40 agonist) in Subjects... | ||
Medical condition: Type 2 Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005125-12 | Sponsor Protocol Number: LIRALUNG | Start Date*: 2016-05-12 |
Sponsor Name:Dr. Albert Lecube, Ph.D., M.D. | ||
Full Title: MULTICENTRE RANDOMIZED DOUBLE BLIND, CROSSOVER, PLACEBO-CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFECT OF LIRAGLUTIDE ON LUNG FUNCTION IN PATIENTS WITH TYPE 2 DIABETES MELLITUS (LIRALUNG STUDY) | ||
Medical condition: Type 2 Diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004990-13 | Sponsor Protocol Number: KRM-307 | Start Date*: 2007-10-17 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation [...] | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of AST-120 for Prevention of Chronic Kidney Disease Progression in Patients with Moderate to Severe Chronic Kidney Disease includin... | |||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004989-17 | Sponsor Protocol Number: KRM-306 | Start Date*: 2007-10-17 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation [...] | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of AST-120 for Prevention of Chronic Kidney Disease Progression in Patients with Moderate to Severe Chronic Kidney Disease | |||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000542-20 | Sponsor Protocol Number: UC-0103/1802 | Start Date*: 2021-01-07 |
Sponsor Name:UNICANCER | ||
Full Title: Randomized phase III study of oral cyclophosphamide vs doxorubicin in 65 years or older patients with advanced or metastatic soft tissue sarcoma: a UNICANCER/GERICO multicenter program | ||
Medical condition: Advanced or metastatic soft tissue sarcoma (STS) in patients ≥65 years old. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003319-21 | Sponsor Protocol Number: PTI-808-01 | Start Date*: 2018-07-20 | |||||||||||
Sponsor Name:Proteostasis Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 1 / 2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PTI-808 in Healthy Adult Subjects and in Adults with Cystic Fibrosis | |||||||||||||
Medical condition: Cystic fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005522-28 | Sponsor Protocol Number: ION363-CS1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 1-3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION363 in Amyotrophic Lateral Sclerosis Patients with Fused in Sarcoma Mutati... | |||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis with Fused in Sarcoma mutations | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) SE (Trial now transitioned) IE (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004854-29 | Sponsor Protocol Number: S245.4.008 | Start Date*: 2007-09-21 | |||||||||||
Sponsor Name:Abbott Products GmbH | |||||||||||||
Full Title: One week double-blind, randomized, placebo-controlled, parallel-group, multi-center study with Creon® 25000 Minimicrospheres™ in subjects with pancreatic exocrine insufficiency after pancreatic sur... | |||||||||||||
Medical condition: Pancreatic Exocrine Insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) BG (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004047-20 | Sponsor Protocol Number: NN1250-4419 | Start Date*: 2018-08-28 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A randomised, cross-over, open-label, multi-centre trial comparing the effect of insulin degludec and insulin glargine 100U/mL, with or without OADs in subjects with type 2 diabetes using flash glu... | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
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