- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Hepatic flexure.
Displaying page 1 of 1.
| EudraCT Number: 2009-015077-12 | Sponsor Protocol Number: rrk3681 | Start Date*: 2009-11-23 |
| Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||
| Full Title: The use of corticosteroids (Budenofalk) as a chemopreventative agent in ulcerative colitis associated neoplasia | ||
| Medical condition: chronic ulcerative colitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003304-39 | Sponsor Protocol Number: 007 | Start Date*: 2019-01-23 | ||||||||||||||||
| Sponsor Name:Morten Rasmussen | ||||||||||||||||||
| Full Title: Efficacy of a novel 1l PEG plus ascorbate (Plenvu) bowel preparation vs. 2l PEG plus ascorbate (Moviprep), a randomized controlled multicenter trial | ||||||||||||||||||
| Medical condition: Bowel preparation before colonoscopy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-000347-60 | Sponsor Protocol Number: TTD-18-01 | Start Date*: 2018-08-08 | |||||||||||
| Sponsor Name:Grupo de Tratamiento de los Tumores Digestivos (TTD) | |||||||||||||
| Full Title: Phase III randomized sequential open-label study to evaluate the efficacy of FOLFOX + panitumumab followed by FOLFIRI + bevacizumab (Sequence 1) versus FOLFOX + bevacizumab followed by FOLFIRI + pa... | |||||||||||||
| Medical condition: metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000939-33 | Sponsor Protocol Number: MLN0002-3026 | Start Date*: 2015-11-11 | |||||||||||
| Sponsor Name:Takeda Development Centre Europe, Ltd. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Double-Dummy, Multicenter, Active-Controlled Study to Evaluate the Efficacy and Safety of Vedolizumab IV Compared to Adalimumab SC in Subjects With Ulcerative Colitis | |||||||||||||
| Medical condition: Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SK (Completed) NL (Completed) BG (Completed) GB (Completed) DE (Completed) HU (Completed) BE (Completed) ES (Completed) LV (Completed) EE (Completed) LT (Completed) PL (Completed) DK (Completed) PT (Completed) HR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001776-15 | Sponsor Protocol Number: MS202202-0002 | Start Date*: 2020-11-16 | |||||||||||
| Sponsor Name:Merck Healthcare KGaA | |||||||||||||
| Full Title: A Phase II single-arm study to investigate tepotinib combined with cetuximab in RAS/BRAF wild-type left-sided metastatic colorectal cancer (mCRC) patients having acquired resistance to anti-EGFR... | |||||||||||||
| Medical condition: left-sided metastatic colorectal cancer (mCRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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