- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
8 result(s) found for: Bismuth.
Displaying page 1 of 1.
| EudraCT Number: 2007-007652-34 | Sponsor Protocol Number: Bismuth-PBH-2008 | Start Date*: 2009-03-05 | |||||||||||
| Sponsor Name:Herlev Hospital, Dept. of haematology (L121) | |||||||||||||
| Full Title: Kan mineraltilskud med bismuth mindske toksiciteten af kemoterapi og strålebehandling? En klinisk prospektiv, dobbeltblind randomiseret undersøgelse af patienter med hæmatologiske sygdomme som modt... | |||||||||||||
| Medical condition: Malignant diseases of the blood requiring chemotherapy and/or radiation therapy of head and neck | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000228-24 | Sponsor Protocol Number: MANA2016-1 | Start Date*: 2016-07-13 |
| Sponsor Name:UZ Brussel | ||
| Full Title: Eradication of H. pylori infection in Belgium: bismuth versus first line therapy | ||
| Medical condition: Patients with H. pylori infection, never treated before | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003931-30 | Sponsor Protocol Number: CBS-EAM-10d | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola | |||||||||||||
| Full Title: A prospective open-label study on efficacy and tolerability of colloidal bismuth sub-citrate as adjunctive therapy to a combination of esomeprazole, amoxicillin and metronidazole for 10 days for He... | |||||||||||||
| Medical condition: Helicobacter pylory infection | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004866-17 | Sponsor Protocol Number: 01/2005 | Start Date*: 2007-04-03 |
| Sponsor Name:Dept Medicine I, Paracelsus Med. Univ. Landeskrankenanstalten Salzburg / SALK | ||
| Full Title: An Open-label, single arm Phase II Trial of Photodynamic Therapy using Foscan for non-curatively-resectable bile duct carcinoma | ||
| Medical condition: Nonresectable hilar or extrahepatic bile duct carcinoma in clinical stage MO ( without liver or peritoneal metastases according to clinical or surgical staging) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006280-78 | Sponsor Protocol Number: PYLHp07-01 | Start Date*: 2008-03-28 | ||||||||||||||||
| Sponsor Name:Axcan Pharma Inc. | ||||||||||||||||||
| Full Title: Efficacy and Safety of Quadruple Therapy by Bismuth Subcitrate Potassium, Metronidazole, and Tetracycline Given x 10 days With Omeprazole in Eradication of Helicobacter pylori: A Comparison to Omep... | ||||||||||||||||||
| Medical condition: Helicobacter pylori infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) GB (Completed) IE (Completed) DE (Completed) NL (Completed) PL (Completed) IT (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-006171-20 | Sponsor Protocol Number: | Start Date*: 2007-05-22 |
| Sponsor Name:CHU Angers | ||
| Full Title: Evaluation de l'efficacité de la thérapie photodynamique par Photofrin sur les cholangiocarcinomes non résécables de type III ou IV | ||
| Medical condition: Cholangiocarcinomes de type III ou IV (selon la classification de Bismuth), prouvé histologiquement. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019064-36 | Sponsor Protocol Number: MA-PY-Hp09-01 | Start Date*: 2011-07-17 | |||||||||||
| Sponsor Name:Axcan Pharma INC | |||||||||||||
| Full Title: Eficacia y seguridad de PYLERA (subcitrato potásico de bismuto, metronidazol y clorhidrato de tetraciclina) con omeprazol, administrados 10 días en sujetos con fracaso del tratamiento de erradicaci... | |||||||||||||
| Medical condition: erradicación de Helicobacter pylori | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-003990-10 | Sponsor Protocol Number: PHOCCC04-01 | Start Date*: 2005-01-18 | |||||||||||
| Sponsor Name:Axcan Pharma Inc. (Axcan Pharma International B.V. is a subsidiary of Axcan Pharma Inc.) | |||||||||||||
| Full Title: Multicenter, open-label, randomised, controlled phase III clinical study of the efficacy and safety of photodynamic therapy using porfimer sodium for injection as palliative treatment for unresecta... | |||||||||||||
| Medical condition: Unresectable Cholangiocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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