- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
20 result(s) found for: Urea breath test.
Displaying page 1 of 1.
EudraCT Number: 2012-000064-24 | Sponsor Protocol Number: AB2012-UBT01 | Start Date*: 2012-07-12 | |||||||||||
Sponsor Name:AB ANALITICA SRL | |||||||||||||
Full Title: Comparative assessment of diagnostic performance of C13-Urea Breath Test (BREATHQUALITY-UBT, oral solution C13-Urea 75 mg/10 mL) with 10 min protocol vs standard 30 min protocol to determinate the ... | |||||||||||||
Medical condition: Presence of symptoms referable to the proximal segment of the digestive system, indicative of a possible Helicobacter pylori infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001598-33 | Sponsor Protocol Number: PSC-DS-BRETEX | Start Date*: 2016-07-27 | |||||||||||
Sponsor Name:SOFAR S.P.A. | |||||||||||||
Full Title: Comparison of two methods for in vivo diagnosis of Helicobacter pylori infection, by means of a tablet of 13C-Urea. | |||||||||||||
Medical condition: H. pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003577-74 | Sponsor Protocol Number: 1.1 | Start Date*: 2007-09-21 | |||||||||||||||||||||
Sponsor Name:University of Nottingham | |||||||||||||||||||||||
Full Title: Helicobacter pylori Eradication vs Aspirin Toxicity Trial Pilot Study | |||||||||||||||||||||||
Medical condition: We are looking at the level of aspirin-associated ulcer bleeds. We are investigating the level of H. pylori infection in aspirin users. People who are positive will be offered eradication treatment. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000789-35 | Sponsor Protocol Number: HPTM06/J/05 | Start Date*: 2006-10-06 |
Sponsor Name:INFAI GmbH | ||
Full Title: Two-way Crossover Comparison of the Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal vs. Standard 13C-Urea Breath Test in Helicobacter Pylori Positive and Neg... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) without interuption of medication two weeks prior to test. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001633-42 | Sponsor Protocol Number: hp001 | Start Date*: 2005-01-06 |
Sponsor Name:NHS GRAMPIAN | ||
Full Title: Is there a role for Helicobacter pylori eradication in the treatment of laryngopharyngeal reflux? : A double blinded randomised case controlled clinical trial | ||
Medical condition: LARYNGOPHARYNGEAL ACID REFLUX | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011979-76 | Sponsor Protocol Number: 253/09 | Start Date*: 2009-04-20 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Effectiveness of acetylcysteine in rescue therapy for Helicobacter pylori infection. Pilot Study | ||||||||||||||||||
Medical condition: Duodenal and gastric ulcer recurrence with Helicobacter P. infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011978-15 | Sponsor Protocol Number: 252/09 | Start Date*: 2010-02-22 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Effectiveness of acetylcysteine in first line therapy to cure Helicobacter pylori. Pilot study. | ||||||||||||||||||
Medical condition: peptic, duodenal and gastric ulcer with Helicobacter pylori infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001401-41 | Sponsor Protocol Number: TAPAS-2014 | Start Date*: 2014-07-29 |
Sponsor Name: | ||
Full Title: Targeting Antibiotics to Pseudomonas Aeruginosa in Small airways (TAPAS) study in patients with cystic fibrosis | ||
Medical condition: Cystic Fibrosis and chronic infection with Pseudomonas aeruginosa | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001369-25 | Sponsor Protocol Number: HPT30/J/17 | Start Date*: 2018-03-19 |
Sponsor Name:INFAI Institut für biomedizinische Analytik und NMR Imaging GmbH | ||
Full Title: The Sensitivity and Specificity of the Modified Helicobacter Test INFAI Using New Test Meal with 13C-Urea Breath Test in Helicobacter Pylori Positive and Negative Patients with Dyspepsia and GERD T... | ||
Medical condition: Diagnosis of Helicobacter pylori infection for patients taking proton pump inhibitors (PPI) with one day break of medication instead of two weeks prior to the test | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003511-31 | Sponsor Protocol Number: V99P2 | Start Date*: 2008-07-16 |
Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | ||
Full Title: Phase I/II, Randomized, Observer-blind, Placebo-controlled, Single-Center Study of the Tolerability, Immunogenicity and Efficacy (following Helicobacter pylori infectious challenge) of Novartis’ In... | ||
Medical condition: no medical condition: healthy subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007749-11 | Sponsor Protocol Number: FINA-002 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:MerLion Pharmaceuticals GmbH | |||||||||||||
Full Title: An open-label, randomized, multicenter, two-arm efficacy and safety study of 14 days treatment with Finafloxacin 400 mg b.i.d. plus Amoxicillin 1000 mg b.i.d. versus Finafloxacin 400 mg b.i.d. plus... | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024644-15 | Sponsor Protocol Number: 2010-024644-15 | Start Date*: 2012-02-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA' DEGLI STUDI DI NAPOLI | |||||||||||||
Full Title: Concomitant therapy with levofloxacyn versus sequential therapy with levofloxacin for eradication of H. pylori infection | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011865-10 | Sponsor Protocol Number: FINA-004 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:MerLion Pharmaceuticals GmbH | |||||||||||||
Full Title: An Open-label, Randomised, Multicentre, Multi-country Three-arm Study of the Treatment with Finafloxacin 400 mg b.i.d. plus Esomeprazole 40 mg b.i.d. for 14 days versus Finafloxacin 400 mg b.i.d. p... | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Prematurely Ended) LV (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002245-36 | Sponsor Protocol Number: MKC-TI-103 | Start Date*: 2006-12-01 | |||||||||||
Sponsor Name:MannKind Corporation | |||||||||||||
Full Title: A Phase 3, 24-Week, Multi-Center, Open-Label, Randomized, Controlled Trial Comparing the Efficacy and Safety of Prandial Inhalation of Technosphere®/Insulin in Combination with Metformin or Technos... | |||||||||||||
Medical condition: Diabetes mellitus type II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006046-17 | Sponsor Protocol Number: E3810-G000-302 | Start Date*: 2008-08-01 | |||||||||||
Sponsor Name:Eisai Limited [...] | |||||||||||||
Full Title: A Randomized Double-Blind Parallel Study of Rabeprazole Extended-Release 50 mg Versus Esomeprazole 40 mg for Healing and Symptomatic Relief of Moderate to Severe Erosive gastroesophageal Reflux Dis... | |||||||||||||
Medical condition: Erosive gastro-oesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) DE (Completed) HU (Completed) FR (Completed) EE (Completed) LT (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005570-32 | Sponsor Protocol Number: E3810-G000-301 | Start Date*: 2008-08-01 | |||||||||||
Sponsor Name:Eisai Limited [...] | |||||||||||||
Full Title: A Randomized Double-Blind Parallel Study of Rabeprazole Extended-Release 50 mg Versus Esomeprazole 40 mg for Healing and Symptomatic Relief of Moderate to Severe Erosive gastroesophageal Reflux Dis... | |||||||||||||
Medical condition: Erosive gastro-oesophageal reflux disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) DE (Completed) HU (Completed) FR (Completed) EE (Completed) LT (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001650-26 | Sponsor Protocol Number: AnticholiumperSeIII | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:Ruprecht-Karls-University Heidelberg, Med Faculty represented by Universitätsklinikum Heidelberg and its Commercial D | |||||||||||||
Full Title: A randomised, placebo-controlled, double-blind, monocentre study on the application of physostigminsalicylate (Anticholium®) as adjunctive measure in perioperative sepsis/septic shock | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003597-10 | Sponsor Protocol Number: CRH103390 | Start Date*: 2006-11-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: Study CRH103390: A 12 Week Flexible Dose Study of GW876008, Placebo and Active Control (Paroxetine) in the Treatment of Social Anxiety Disorder (SocAD) | |||||||||||||
Medical condition: Social Anxiety Disorder (SocAD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
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: 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 |
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