- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Bile salts.
Displaying page 1 of 1.
EudraCT Number: 2016-002965-67 | Sponsor Protocol Number: 57877.018.016 | Start Date*: 2017-07-07 | |||||||||||
Sponsor Name:AMC | |||||||||||||
Full Title: An open, non-randomized, parallel-group pharmokinetic and -dynamic, investigator-initiated study on effects of obeticholic acid (OCA) in bile of patients with primary biliary cholangitis (PBC) and ... | |||||||||||||
Medical condition: Primary biliairy cholangitis (PBC) Non-alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001200-20 | Sponsor Protocol Number: CSET 1287 | Start Date*: 2007-06-01 |
Sponsor Name:Institut Gustave Roussy | ||
Full Title: A Multicenter, Randomized Phase II Trial Assessing the Activity of Gemcitabine – Oxaliplatin Chemotherapy Alone or in Combination with Cetuximab in Patients with Advanced Biliary Cancer | ||
Medical condition: adenocarcinoma of the biliary tract ( gallbladder, intra and/ or extrahepatic bile ducts, ampulla of Vater) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005387-10 | Sponsor Protocol Number: ERY-PAO | Start Date*: 2013-03-27 |
Sponsor Name:Department of hospital Pharmacy, Medical Centre Haaglanden | ||
Full Title: Effect of Roux-en-Y gstric bypass surgery in morbidly obese patients on Pharmacokinetics of (Acetyl)salicylic acid and Omeprazole. | ||
Medical condition: Roux-en-Y gastric bypass (RYGB) surgery is a successful treatment for morbid obesity. In this procedure, a small gastric pouch is created. The duodenum is bypassed by connecting the jejunum to this... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003141-10 | Sponsor Protocol Number: AGO/2014/004 | Start Date*: 2014-09-29 | ||||||||||||||||
Sponsor Name:Ghent University Hospital | ||||||||||||||||||
Full Title: Invloed van UDCA op fecale galzoutensamenstelling van IBD patiënten: piloot studie. | ||||||||||||||||||
Medical condition: Crohn's disease or colitis ulcerosa | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005796-34 | Sponsor Protocol Number: CC-GEMSO-2007 | Start Date*: 2008-03-19 | |||||||||||
Sponsor Name:Universität Mainz, I. Medizinische Klinik und Poliklinik | |||||||||||||
Full Title: A randomized, double-blind, multicenter phase II trial with gemcitabine plus sorafenib versus gemcitabine plus placebo in patients with chemo-naive advanced or metastatic adenocarcinoma of the bili... | |||||||||||||
Medical condition: Patients with Adenocarcinoma of the gallbladder or intrahepatic bile ducts or histologically proven hepatic metastases of an earlier resected and histologically proven biliary tract cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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