- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
58 result(s) found for: Lower gastrointestinal tract.
Displaying page 1 of 3.
EudraCT Number: 2007-004127-38 | Sponsor Protocol Number: TILATT/0708 | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: USE OF ORAL TILACTASE ENZYMES IN SUBJECTS WITH LACTOSE MALABSORPTION AND INTOLERANCE. CLINICAL RELEVANCE IN A POPULATION WITH HIGH PREVALENCE OF LACTASE DEFICIENCY IN SOUTHERN ITALY. | |||||||||||||
Medical condition: primary lactase deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002418-22 | Sponsor Protocol Number: T-016 | Start Date*: 2014-11-07 | ||||||||||||||||||||||||||
Sponsor Name:Trio Medicines Ltd | ||||||||||||||||||||||||||||
Full Title: Randomized, placebo-controlled trial of YF476, a gastrin receptor antagonist, in Barrett’s esophagus (10-505; T-016) | ||||||||||||||||||||||||||||
Medical condition: Barrett's oesophagus | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001097-24 | Sponsor Protocol Number: PHT/2013/01 | Start Date*: 2013-05-23 | |||||||||||
Sponsor Name:Portsmouth Hospitals NHS trust | |||||||||||||
Full Title: Use of N-Acetylcysteine (NAC) and Simeticone as a pre-endoscopic drink to improve mucosal visualisation during gastroscopy: A randomised controlled trial | |||||||||||||
Medical condition: Early gastrointestinal lesions in the upper gastrointestinal tract. Our study is not looking at the direct treatment of any particular condition, but the early detecton of lesions. When performin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003637-14 | Sponsor Protocol Number: AGO/2018/004 | Start Date*: 2019-03-29 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Local injection of collagenase clostridium histolyticum (XiapexR) for refractory gastrointestinal strictures: an open-label pilot study. | |||||||||||||
Medical condition: refractory iatrogenic gastrointestinal strictures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001684-36 | Sponsor Protocol Number: GED0507-UC-001 | Start Date*: 2016-12-12 | ||||||||||||||||||||||||||
Sponsor Name:PPM SERVICES SA | ||||||||||||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, PLACEBO-CONTROLLED, MULTICENTER STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF GED-0507-34-LEVO (GED0507) FOR TREATMENT OF SUBJECTS WITH ACTIVE ULCERATIVE COLITIS | ||||||||||||||||||||||||||||
Medical condition: Ulcerative Colitis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) HU (Prematurely Ended) BG (Prematurely Ended) LV (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002624-28 | Sponsor Protocol Number: FIT-EU-04 | Start Date*: 2015-09-24 |
Sponsor Name:Nutrinia Ltd. | ||
Full Title: A Multi-center, Double-blind, Randomized Placebo Controlled Study to Assess the Efficacy and Safety of NTRA-2112 on Gastrointestinal Maturation in Preterm Infants. | ||
Medical condition: Gastrointestinal Maturation in Preterm Infants. | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) BE (Completed) NL (Prematurely Ended) GB (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) BG (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-004588-29 | Sponsor Protocol Number: TA799-101 | Start Date*: 2022-02-01 | ||||||||||||||||||||||||||
Sponsor Name:VectivBio AG | ||||||||||||||||||||||||||||
Full Title: A randomized, single-blind trial to evaluate the safety and efficacy of apraglutide in subjects with Grade II to IV (MAGIC) steroid refractory gastrointestinal (GI) acute graft versus host disease ... | ||||||||||||||||||||||||||||
Medical condition: Acute graft versus host disease (aGVHD) | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PT (Prematurely Ended) FR (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014845-95 | Sponsor Protocol Number: NRL0706-01/2009 (VOM) | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:Norgine Ltd. | |||||||||||||
Full Title: Open study to assess the tolerability, safety and efficacy of an adapted 2 litre gut cleansing solution (NRL0706) in routine colon cleansing prior to colonoscopies for colon tumour screening | |||||||||||||
Medical condition: Subjects without relevant clinical symptoms for gastrointestinal disorders will undergo a complete selective colonoscopy for colon cancer screening. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008857-53 | Sponsor Protocol Number: DC10004 | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:Acacia Pharma Ltd | |||||||||||||
Full Title: Open-Label, Pilot Phase I/II Study of the Efficacy and Safety of Concomitant Megestrol + Formoterol in Patients with Cachexia and Advanced Malignancy | |||||||||||||
Medical condition: Cancer-related cachexia, also known as Cancer Anorexia-Cachexia Syndrome (CACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002302-39 | Sponsor Protocol Number: RSV-M-301 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:Novavax, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a Respiratory Syncytial Virus (RSV) F Nanoparticle Vaccine with Alumi... | |||||||||||||
Medical condition: Respiratory syncytial virus (RSV) is the leading viral cause of severe lower respiratory tract disease in infants and young children worldwide. In industrialized countries, nearly all children have... | |||||||||||||
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Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021879-85 | Sponsor Protocol Number: 10050 | Start Date*: 2010-09-08 |
Sponsor Name:University of Nottingham | ||
Full Title: Mode of action of Moviprep:impact on distribution of intestinal fluid and colonic microbiota | ||
Medical condition: for bowel cleansing prior to any clinical procedure requiring a clean bowel, e.g, bowel endoscopy, lower gastrointestinal tract radiology or digestive tract surgery. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001841-11 | Sponsor Protocol Number: MPOH06 | Start Date*: 2021-11-09 | |||||||||||
Sponsor Name:MaaT Pharma | |||||||||||||
Full Title: Evaluation of the efficacy of MaaT013 as salvage therapy in acute GVHD patients with gastrointestinal involvement, refractory to ruxolitinib; a multi-center open-label phase III trial | |||||||||||||
Medical condition: Salvage therapy of acute GVHD patients with gastrointestinal involvement, refractory to ruxolitinib. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005688-26 | Sponsor Protocol Number: Abstral | Start Date*: 2012-02-01 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Procedural pain treatment with transmucosal sublingual fentanyl tablet in colonoscopy patients | |||||||||||||
Medical condition: Patients undergoing colonoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001749-15 | Sponsor Protocol Number: ARC005 | Start Date*: 2019-05-21 | |||||||||||
Sponsor Name:Aimmune Therapeutics , Inc. | |||||||||||||
Full Title: Peanut Oral Immunotherapy Study of Early Intervention for Desensitization (POSEIDON) | |||||||||||||
Medical condition: Peanut Allergy | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005547-17 | Sponsor Protocol Number: RHMNUT0048 | Start Date*: 2010-01-28 |
Sponsor Name:Southampton University Hospital NHS Trust | ||
Full Title: Refeeding risks in patients requiring nutrition support. A twin centre double-blind randomised controlled trial of parenteral nutrition support. | ||
Medical condition: Patients who have a non-functioning gastrointestinal tract require artifical intravenous nutrition. This is usally a result recent surgery or sepsis causing a reversible short term paralysis of th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001976-48 | Sponsor Protocol Number: IM011023 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of BMS-986165 in Subjects with Moderate to Severe Crohn's Disease | ||||||||||||||||||
Medical condition: Crohn's Disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) FR (Completed) ES (Ongoing) PL (Completed) DE (Completed) DK (Prematurely Ended) PT (Completed) NL (Completed) BE (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004217-26 | Sponsor Protocol Number: CSUC-01/16 | Start Date*: 2017-04-21 |
Sponsor Name:InDex Pharmaceuticals AB | ||
Full Title: A Randomised Dose-Optimisation Study to Evaluate the Efficacy and Safety of Cobitolimod in Moderate to Severe Active Ulcerative Colitis Patients | ||
Medical condition: Moderate to Severe left-sided Active Ulcerative Colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) SE (Completed) ES (Completed) CZ (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000326-58 | Sponsor Protocol Number: ARC009 | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Aimmune Therapeutics, Inc. | |||||||||||||
Full Title: Peanut Allergy Oral Immunotherapy Study of AR101 for Desensitization in Children and Adolescents: Real-World, Open-Label, Quality of Life Study | |||||||||||||
Medical condition: Peanut Allergy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IE (Prematurely Ended) SE (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004581-14 | Sponsor Protocol Number: A3921139 | Start Date*: 2012-06-29 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL STUDY OF CP-690,550 IN SUBJECTS WITH MODERATE TO SEVERE ULCERATIVE COLITIS | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DK (Completed) HU (Completed) EE (Completed) GB (Completed) LV (Completed) BE (Completed) NL (Completed) ES (Completed) AT (Completed) DE (Completed) SK (Completed) PL (Completed) IT (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005575-34 | Sponsor Protocol Number: P060240 | Start Date*: 2008-02-08 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Comparaison de la tolérance et de l'acceptabilité de la coloscopie sous sédation par mélange équimolaire d'oxygène et de protoxyde d'azote par rapport à l'anesthésie générale : Etude randomisée mul... | |||||||||||||
Medical condition: maladies digestives. | |||||||||||||
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Population Age: Adults, Elderly | Gender: | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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