- Trials with a EudraCT protocol (1,082)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (600)
1,082 result(s) found for: Digestive System Diseases.
Displaying page 5 of 55.
EudraCT Number: 2020-000483-27 | Sponsor Protocol Number: CCT38473 | Start Date*: 2020-11-19 |
Sponsor Name:St. Joseph’s Healthcare, McMaster University | ||
Full Title: Re-Evaluating the Inhibition of Stress Erosions: Gastrointestinal Bleeding Prophylaxis in ICU | ||
Medical condition: critical illness requiring mechanical ventilation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001472-18 | Sponsor Protocol Number: UDT-2/PHT | Start Date*: 2011-05-10 |
Sponsor Name:STZ 1172 Gesundheitsförderung und Stoffwechselforschung | ||
Full Title: Double-Blind, Randomised, Cross-Over, Placebo-Controlled, Single-Centre Phase IIa Clinical Study on the Influence of Udenafil on the Portal Flow in Cirrhotic Patients with Portal Hypertension | ||
Medical condition: Portal hypertension, liver cirrhosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004228-70 | Sponsor Protocol Number: IBP-9414-010 | Start Date*: 2015-12-28 |
Sponsor Name:Infant Bacterial Therapeutics AB | ||
Full Title: A randomized, double blind, parallel-group, dose escalation placebo-controlled multicentre study to investigate the safety and tolerability of IBP-9414 administered in preterm infants | ||
Medical condition: Prevention of necrotizing enterocolitis in preterm infants with birth weight less than or equal to 1,500 grams | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002900-15 | Sponsor Protocol Number: Transidose-GE_01/2013 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:Salsarulo Pharma | |||||||||||||
Full Title: Clinical trial to evaluate the efficacy and safety of oral Transidose in patients suffering from constipation. | |||||||||||||
Medical condition: Constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003192-30 | Sponsor Protocol Number: CLJN452X2202 | Start Date*: 2016-03-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A double blind, randomized placebo controlled crossover multiple dose study of LJN452 to assess safety, tolerability and efficacy in patients with primary bile acid diarrhea (pBAD). | |||||||||||||
Medical condition: primary bile acid diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005467-32 | Sponsor Protocol Number: n.a. | Start Date*: 2016-08-08 |
Sponsor Name:Haga Teaching Hospital | ||
Full Title: A randomised controlled trial on the effect of laxative therapy in children with functional abdominal pain | ||
Medical condition: Functional abdominal pain | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004355-23 | Sponsor Protocol Number: PPI-microbiome-FD | Start Date*: 2018-01-04 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome in Functional Dyspepsia patients | ||
Medical condition: Functional Dyspepsia (FD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002601-19 | Sponsor Protocol Number: OND-URG | Start Date*: 2019-09-16 |
Sponsor Name:Basque Health Service | ||
Full Title: Effectiviness and safety of the administration of ondansetron versus placebo for the treatment of vomit in children with mild and moderate dehydration: randomized clinical trial | ||
Medical condition: Vomiting | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003129-92 | Sponsor Protocol Number: 11-1-039 | Start Date*: 2012-06-04 |
Sponsor Name:MUMC+ | ||
Full Title: The Orange III trial: Optimised recovery with Movicol preoperatively within an enhanced recovery programme, a randomised controlled trial | ||
Medical condition: Liver resection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004629-42 | Sponsor Protocol Number: ENTER_L_01125 | Start Date*: 2015-04-03 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Bacillus Clausii in Preventing Antibiotic-Associated Diarrhea Among Filipino Infant and Children: A Multi-Center, Randomized, Open-Label Controlled (Treatment vs No Treatment) Clinical Trial of Eff... | |||||||||||||
Medical condition: Diarrhea associated to antibiotics | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002408-34 | Sponsor Protocol Number: Nosponsor | Start Date*: 2011-10-05 | |||||||||||
Sponsor Name:Matti Ristikankare | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001503-37 | Sponsor Protocol Number: AZA/allo/v2.29.03.2013 | Start Date*: 2013-05-31 | |||||||||||
Sponsor Name:Marianne Kiszka-Kanowitz | |||||||||||||
Full Title: Effect of low-dose Azathioprine and Allopurinol compared to Azathioprine on clinical outcomes in Inflammatory Bowel Disease | |||||||||||||
Medical condition: Inflammatory Bowel Disease, (Ulcerativ colitis, Crohns disease) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004268-31 | Sponsor Protocol Number: 20110118 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Adalimumab (Humira) in the treatment of chronic pouchitis | |||||||||||||
Medical condition: Chronic pouchitis after proctocolectomy and reconstruction with a J-pouch and with ulcerative colitis as primary diagnosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000406-30 | Sponsor Protocol Number: 3071-305-020 | Start Date*: 2020-07-13 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: Open-label Extension Study of Relamorelin for the Treatment of Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001776-19 | Sponsor Protocol Number: 2010-19 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bombastus-Werke AG | |||||||||||||
Full Title: MULTICENTRIC RANDOMIZED PLACEBO-CONTROLLED DOUBLE-BLIND 2-ARM PIVOTAL STUDY ON EFFICACY AND SAFETY OF ARHAMA®-TINKTUR N IN PATIENS WITH ACUTE DIARRHEA | |||||||||||||
Medical condition: Acute unspecific diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000515-80 | Sponsor Protocol Number: RIFA-AAH | Start Date*: 2012-08-29 | |||||||||||
Sponsor Name:Juan Córdoba | |||||||||||||
Full Title: Effects of rifaximin administration in patients with severe acute alcoholic hepatitis. Comparative pilot study. | |||||||||||||
Medical condition: Acute alcoholic hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003174-89 | Sponsor Protocol Number: AUDC/11 | Start Date*: 2013-01-28 | |||||||||||
Sponsor Name:Enrique De Madaria Pascual | |||||||||||||
Full Title: Ursodeoxycholic acid in the secondary prophylaxis of acute biliary pancreatitis: pilot clinical trial randomized double-blind. | |||||||||||||
Medical condition: Gallstone Dissolution | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005059-10 | Sponsor Protocol Number: Trp-IBD | Start Date*: 2018-09-14 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Multicentric, double-blind, placebo controlled clinical trial with 5-hydroxytryptophan (5-HTP) in patients with inflammatory bowel disease in clinical and biologic remission: effect on fatigue scores | ||
Medical condition: Inflammatory Bowel Disease (IBD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001856-51 | Sponsor Protocol Number: 12.007 | Start Date*: 2014-08-26 | |||||||||||
Sponsor Name:Aleksander Krag | |||||||||||||
Full Title: Anti-fibrotic and molecular aspects of rifaximin in alcoholic liver disease: A randomized placebo controlled clinical trial | |||||||||||||
Medical condition: Liver fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001355-12 | Sponsor Protocol Number: LPS15198 | Start Date*: 2019-02-27 | |||||||||||
Sponsor Name:SANOFI-AVENTIS GROUPE | |||||||||||||
Full Title: Phase IV, randomized, double-blind, multicenter, placebo-controlled clinical trial to evaluate the efficacy and the safety of enterogermina (Bacillus clausii) in treating patients with small intest... | |||||||||||||
Medical condition: Small intestinal bacterial overgrowth (SIBO) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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