- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Food groups.
Displaying page 1 of 3.
EudraCT Number: 2018-004427-37 | Sponsor Protocol Number: 5421234 | Start Date*: 2019-02-20 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Odense Research Centre for Anaphylaxis (ORCA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Treatment with Omalizumab in food allergic children | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Food Allergy with Anaphylaxis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000841-28 | Sponsor Protocol Number: DC2017DECREASE01 | Start Date*: 2017-08-14 |
Sponsor Name:VU University Medical Center | ||
Full Title: Combined effects of SGLT2 inhibition and GLP-1 receptor agonism on food intake, body weight and central satiety and reward circuits in obese T2DM patients | ||
Medical condition: Type 2 diabetes mellitus Obesity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000276-10 | Sponsor Protocol Number: FAST2015 | Start Date*: 2015-07-02 |
Sponsor Name:FAST Consortium under EU 7. FWP | ||
Full Title: FAST – Food Allergy Specific ImmunoTherapy A multinational phase IIb study to investigate the efficacy and safety of subcutaneous immunotherapy with a modified fish- parvalbumin given in single ri... | ||
Medical condition: Food allergy to fish | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) DK (Completed) GR (Ongoing) NL (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000712-59 | Sponsor Protocol Number: APHP200073 | Start Date*: 2023-03-14 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux Paris (Direction de la Recherche Clinique et de l’Innovation) | |||||||||||||
Full Title: Severe erythema multiforme: A randomized controlled trial comparing a short systemic corticosteroids regimen to placebo in the acute established phase | |||||||||||||
Medical condition: Erythema multiforme (EM) in its severe form managed at the hospital | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001786-12 | Sponsor Protocol Number: CDX0159-08 | Start Date*: 2023-03-31 | |||||||||||
Sponsor Name:Celldex Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Barzolvolimab (CDX-0159) in Adults with Active Eosinophilic Esophagitis (The "EvolvE" Study) | |||||||||||||
Medical condition: Eosinophilic esophagitis (EoE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002968-10 | Sponsor Protocol Number: 024 | Start Date*: 2008-01-17 |
Sponsor Name:Department of Medicine I, Clinical Dep. f. Oncology, University Hospital, | ||
Full Title: Treatment of Patients Suffering from Tumour Cachexia with Dronabinol (tetrahydrocannabinol) or Placebo Comparison of individually optimised dosages in a double blind, randomised parallel design | ||
Medical condition: tumour cachexia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005306-39 | Sponsor Protocol Number: VitaminKStudy | Start Date*: 2009-06-29 | |||||||||||
Sponsor Name:RWTH Aachen University, represented by the rector, himself represented by Clinical Trial Center Aachen (CTC-A) | |||||||||||||
Full Title: Food supplementation with Vitamin K for MGP-activation and inhibition of progression of aortic valve calcification | |||||||||||||
Medical condition: progression of aortic valve calcification | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004150-17 | Sponsor Protocol Number: 341-15 | Start Date*: 2015-12-11 |
Sponsor Name:Västra Götalandsregionen | ||
Full Title: The Effect of Satiety Gut Hormone Modulation on Appetitive Drive After Upper Gastrointestinal Surgery | ||
Medical condition: Weight loss and malnutrition after curative surgery for upper gastrointestinal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001628-45 | Sponsor Protocol Number: 2.0 | Start Date*: 2015-09-09 |
Sponsor Name:Dep. of Medical Cell Biology Uppsala University | ||
Full Title: A parallel, double-blinded, randomized, 6 months, two arms study with lifestyle intervention and exenatide 2 mg once weekly or lifestyle intervention and placebo in adolescents with obesity to expl... | ||
Medical condition: Obesity in adolescents | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003226-25 | Sponsor Protocol Number: Abifood01 | Start Date*: 2013-07-12 | |||||||||||
Sponsor Name:Fundacion Publica Andaluza para la Gestion de la Investigacion en Salud de Sevilla | |||||||||||||
Full Title: Phase I, randomized, open design trial to evaluate the effect of food (fasting, fat meal and standard meal) on the pharmacokinetics of abiraterone acetate at reduced doses, compared with convention... | |||||||||||||
Medical condition: metastatic prostatic cancer after castration-resistant progression to docetaxel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002701-68 | Sponsor Protocol Number: PSN9301CS01 | Start Date*: 2004-12-13 |
Sponsor Name:Prosidion Ltd. | ||
Full Title: A randomised, double-blind, placebo-controlled, multiple dose, time-lagged parallel groups trial, investigating the pharmacodynamics, the safety and tolerability and the pharmacokinetics of PSN9301... | ||
Medical condition: Diabetes mellitus type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003546-16 | Sponsor Protocol Number: 1.2 | Start Date*: 2014-03-20 |
Sponsor Name:Medizinische Universität Wien, Klin. Abt. für Endokrinologie & Stoffwechsel, Universitätsklinik für Innere Medizin III | ||
Full Title: The Link between Obesity And Vitamin D in bariatric patients with omega-loop bypass surgery: a randomized controlled, double-blinded clinical supplementation trial - LOAD | ||
Medical condition: The aim of the study is to increase vitamin D concentrations respectively to keep it on high level by supplementing with cholecalciferol in a different dose regime, and to improve the overall healt... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001054-84 | Sponsor Protocol Number: 2004/W/GI/02 | Start Date*: 2005-02-16 |
Sponsor Name:NHS Lothian- University Hospitals Division | ||
Full Title: A comparison of the efficacy of dietary hydroxypropylcellulose and questran as therapeutic agents in bile acid induced diarrhoea | ||
Medical condition: these patients will have bile acid induced diarrhoea identified by an increased serum 7a-OH-cholestenone. and will have a history of one of 1. ileal resection 2. idiopathic bile acid diarrhoea.3. ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017768-18 | Sponsor Protocol Number: 0908127 | Start Date*: 2010-03-19 | ||||||||||||||||
Sponsor Name:CHU Saint-Etienne | ||||||||||||||||||
Full Title: Analgésie par bloc continu du plan transverse de l’abdomen en chirurgie d’exérèse hépatique : efficacité et influence sur la réhabilitation précoce. | ||||||||||||||||||
Medical condition: hepatectomy or segmentectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000353-65 | Sponsor Protocol Number: N-ISP-1 | Start Date*: 2007-10-23 | |||||||||||
Sponsor Name:University Hospital Tübingen | |||||||||||||
Full Title: Weight gain, eating patterns, and development of body composition during initiation of basal insulin therapy: a comparison of insulin detemir and insulin glargine | |||||||||||||
Medical condition: Typ 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001294-31 | Sponsor Protocol Number: D5244C00001 | Start Date*: 2022-12-06 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Phase 3 Efficacy and Safety Study of Tezepelumab in Patients with Eosinophilic Esophagitis (CROSSING) | |||||||||||||
Medical condition: Eosinophilic esophagitis (EoE) is a rare, chronic inflammatory disorder triggered by an immune response to foods and aeroantigens and characterized by a combination of esophageal dysfunction and eo... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) SE (Trial now transitioned) SK (Trial now transitioned) ES (Ongoing) CZ (Ongoing) DK (Trial now transitioned) GR (Trial now transitioned) FI (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000169-40 | Sponsor Protocol Number: EPaNIC S50404 | Start Date*: 2007-05-10 | ||||||||||||||||
Sponsor Name:Catholic University Leuven | ||||||||||||||||||
Full Title: Impact of early parenteral nutrition completing enteral nutrition in adult critically ill patients | ||||||||||||||||||
Medical condition: Critical Illness | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002550-32 | Sponsor Protocol Number: VIPES | Start Date*: 2012-12-21 | |||||||||||
Sponsor Name:DBV Technologies SA | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized trial to study the Viaskin® Peanut’s Efficacy and Safety for treating peanut allergy in children and adults. | |||||||||||||
Medical condition: Treatment of peanut allergy in adults and children age 6 years and older with documented hypersensitivity to peanut. The induction of clinical desensitization to peanut in patients allergic to pean... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) PL (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005327-16 | Sponsor Protocol Number: | Start Date*: 2014-07-15 | |||||||||||
Sponsor Name:The University of Edinburgh [...] | |||||||||||||
Full Title: A Randomized Open Label Pilot Study to Compare Targinact vs. Oxycodone in Early Return of Gastrointestinal Function after Colorectal Surgery | |||||||||||||
Medical condition: Post-operative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000364-28 | Sponsor Protocol Number: 00/0594-LINARI | Start Date*: 2013-05-16 | |||||||||||
Sponsor Name:Profil Institut für Stoffwechselforschung GmbH | |||||||||||||
Full Title: Effects of Linagliptin on active GLP-1 concentrations in subjects with renal impairment | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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