- Trials with a EudraCT protocol (506)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (28)
506 result(s) found for: Inflammatory bowel disease.
Displaying page 2 of 26.
EudraCT Number: 2022-002751-19 | Sponsor Protocol Number: 82160 | Start Date*: 2023-04-11 |
Sponsor Name:Amsterdam UMC | ||
Full Title: FAPi-PET imaging of in vivo fibrosis in inflammatory bowel disease patients | ||
Medical condition: Inflammatory Bowel Diseases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2022-000894-16 | Sponsor Protocol Number: NL79105.058.22 | Start Date*: 2022-05-04 | |||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
Full Title: Predicting Response to Iron Supplementation in Patients with active Inflammatory Bowel Disease | |||||||||||||||||||||||
Medical condition: Inflammatory Bowel Disease | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000245-12 | Sponsor Protocol Number: Repha_1436 | Start Date*: 2020-01-20 | ||||||||||||||||
Sponsor Name:Repha GmbH | ||||||||||||||||||
Full Title: Controlled clinical trial to evaluate the efficacy and safety of MYRRHINIL-INTEST® versus placebo in patients with diarrhea-dominant irritable bowel syndrome (IBS-D) and patients with mixed-type ir... | ||||||||||||||||||
Medical condition: A confirmed diagnosis of irritable bowel syndrome (IBS-D or IBS-M) by a specialist in gastroenterology and/or internal medicine and/or general medicine | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000985-14 | Sponsor Protocol Number: VICAPEND | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:Universitary Hospital Príncipe de Asturias | |||||||||||||
Full Title: Valuation of visualization quality of mucous membrane and diagnostic yield of small bowel capsule endoscopy using different bowel preparations clinical trial | |||||||||||||
Medical condition: Obscure gastrointestinal bleeding. Inflammatory bowel disease as Crohn's disease. Tumors of the small intestine. Hereditary polyposis syndrome (familial adenomatous polyposis or Peutz-Jeghers Syndr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001593-25 | Sponsor Protocol Number: P-Monofer-IBD-01-Extension | Start Date*: 2011-06-08 | ||||||||||||||||
Sponsor Name:Pharmacosmos A/S | ||||||||||||||||||
Full Title: An Open-label, Multi-Centre, Non-Randomised Extension Study to Assess the Ability to Maintain a Stable Haemoglobin and to Assess Safety of Iron Isomaltoside 1000 (Monofer®) in Subjects with Inflamm... | ||||||||||||||||||
Medical condition: Inflammatory bowel disease subjects with iron deficiency anaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002685-38 | Sponsor Protocol Number: 2-2 | Start Date*: 2005-08-05 |
Sponsor Name:Yakult Honsha Co | ||
Full Title: Randomised controlled trial of metronidazole and probiotic preparation versus placebo in the treatment of irritable bowel syndrome | ||
Medical condition: Irritable Bowel Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003625-46 | Sponsor Protocol Number: SCG01SII | Start Date*: 2006-03-28 | |||||||||||
Sponsor Name:ITALCHIMICI SPA | |||||||||||||
Full Title: EFFICACY OF ORAL SODIUM CROMOGLICATE IN THE IRRITABLE BOWEL SYNDROME: A DOUBLE BLIND PLACEBO CONTROLLED MULTICENTRE RANDOMISED STUDY | |||||||||||||
Medical condition: IRRITABLE BOWEL SYNDROME | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) CZ (Completed) SK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004277-17 | Sponsor Protocol Number: 2008/2 | Start Date*: 2010-05-10 |
Sponsor Name:GlobiFer International bvba | ||
Full Title: The effectiveness and tolerability of GlobiFer (haem iron) tablets compared to ferrous sulphate tablets in inflammatory bowel disease: a randomised-controlled trial. | ||
Medical condition: Anaemia in inflammatory bowel disease | ||
Disease: | ||
Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001919-39 | Sponsor Protocol Number: 48890 | Start Date*: 2014-08-27 |
Sponsor Name:Erasmus MC | ||
Full Title: Lengthening Adalimumab Dosing Interval in IBD patients in long term remission, the LADI study | ||
Medical condition: Inflammatory bowel disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003328-12 | Sponsor Protocol Number: ThromboVIT | Start Date*: 2006-12-11 |
Sponsor Name:Vifor Int. | ||
Full Title: A multi-centre, randomized, controlled, single-blinded, phase II study to investigate the safety and efficacy of intravenous infusions of FERINJECT® versus placebo in patients with thrombocytosis s... | ||
Medical condition: Persons with Inflammatory Bowel Disease, thrombocytosis and iron deficiency | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (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: 2020-004012-10 | Sponsor Protocol Number: MODIFI | Start Date*: 2021-06-17 |
Sponsor Name:UZ Leuven | ||
Full Title: Model-informed infliximab dose de-escalation following earlier dose escalation in adult patients with inflammatory bowel diseases | ||
Medical condition: Inflammatory bowel diseases - Crohn's disease - ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
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: 2019-003987-37 | Sponsor Protocol Number: 2019-001G | Start Date*: 2020-02-26 |
Sponsor Name:University Medical Centre Ljubljana, Department of gastroenterology | ||
Full Title: Exposure-response of golimumab during maintenance in ulcerative colitis: An exploratory Pharmacokinetics/Pharmacodynamics comparison of different dose regimens | ||
Medical condition: Ulcerative colitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000837-17 | Sponsor Protocol Number: NL80854.018.22 | Start Date*: 2022-12-07 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Subcutaneous vedolizumab drug de-escalation using therapeutic drug monitoring in inflammatory bowel disease: a randomized controlled pilot study | ||
Medical condition: Inflammatory bowel diseases (Crohn's disease, ulcerative colitis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002982-20 | Sponsor Protocol Number: 5155 | Start Date*: 2020-01-29 | ||||||||||||||||
Sponsor Name:Royal Liverpool University Hospital | ||||||||||||||||||
Full Title: A Pilot Study to assess the efficacy and safety of reduced dose oral iron in the treatment of iron deficiency anaemia in inflammatory bowel disease patients | ||||||||||||||||||
Medical condition: Iron deficiency anaemia in inflammatory bowel disease | ||||||||||||||||||
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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: 2011-004561-33 | Sponsor Protocol Number: ThromboAct | Start Date*: 2014-05-23 |
Sponsor Name:Medizinische Universität Wien, Klinik für Innere Medizin III, Abteilung für Gastroenterologie und Hepatologie | ||
Full Title: A randomized, controlled, single-blinded, phase II study to investigate the safety and efficacy of intravenous infusions of FERINJECT® versus placebo on platelet activity in patients with iron defi... | ||
Medical condition: iron deficiency in chronic inflammatory bowel disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004399-42 | Sponsor Protocol Number: C87037 | Start Date*: 2015-03-05 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A Phase II, Multi-center, Double-blind, Placebo-controlled, Parallel-group, Dose-response Study to Assess the Safety and Efficacy of CDP870/Certolizumab Pegol, Dosed Subcutaneously in Patients With... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001772-30 | Sponsor Protocol Number: RIDARTII | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:FONDAZIONE I.R.C.C.S. POLICLINICO SAN MATTEO | |||||||||||||
Full Title: Clinical burden of anemia in inflammatory bowel disease: Role of Iron Deficiency And iron Replacement Therapy, therapeutic trial | |||||||||||||
Medical condition: Anemia in inflammatory bowel disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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