- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Hydrogen Breath Test.
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EudraCT Number: 2022-001368-86 | Sponsor Protocol Number: SIBO_SUBSTRAT | Start Date*: 2023-06-14 | ||||||||||||||||
Sponsor Name:Hospital Universitario de La Princesa | ||||||||||||||||||
Full Title: RANDOMIZED, MULTICENTRIC CLINICAL TRIAL, COMPARISON BETWEEN LACTITOL AND LACTULOSE AS SUBSTRATES BREATH TEST FOR THE DIAGNOSIS OF BACTERIAL OVERGROWTH | ||||||||||||||||||
Medical condition: Intestinal bacterial overgrowth | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005312-62 | Sponsor Protocol Number: F60038 GE 401 | Start Date*: 2008-03-21 | |||||||||||
Sponsor Name:Pierre Fabre Médicament | |||||||||||||
Full Title: Etude chez le sujet volontaire sain de l’effet de carbolevure versus placebo sur la fermentation intestinale induite par l’ingestion de lactulose. | |||||||||||||
Medical condition: Observation chez le sujet volontaire sain de la production d’hydrogène secondaire à l’administration de lactulose avec une administration concomitante de carbolevure, association de charbon activé ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001793-15 | Sponsor Protocol Number: Gastro_CHU_16-1 | Start Date*: 2016-07-12 | |||||||||||
Sponsor Name:LactoResearch sprl | |||||||||||||
Full Title: PROSPECTIVE STUDY OF THE EFFICIENCY OF PROBIOTIC MIXTURE TO IMPROVE LACTOSE DIGESTION AND SYMPTOMS OF LACTOSE INTOLERANCE | |||||||||||||
Medical condition: lactose intolerance | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001181-26 | Sponsor Protocol Number: VPH-GXL-2013-01 | Start Date*: 2015-07-16 |
Sponsor Name:Venter Pharma S.L. | ||
Full Title: Evaluation of the impact of LacTEST on diagnostic thinking and on patient management, and of the reproducibility (Test-Retest), for the diagnosis of hypolactasia in adults and elderly patients pres... | ||
Medical condition: Evaluación del impacto de LacTEST en el pensamiento diagnóstico y en el manejo terapéutico del paciente, y de reproducibilidad (Test-Retest), para el diagnóstico de la hipolactasia en adultos y pob... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001355-12 | Sponsor Protocol Number: LPS15198 | Start Date*: 2019-02-27 | |||||||||||
Sponsor Name:SANOFI-AVENTIS GROUPE | |||||||||||||
Full Title: Phase IV, randomized, double-blind, multicenter, placebo-controlled clinical trial to evaluate the efficacy and the safety of enterogermina (Bacillus clausii) in treating patients with small intest... | |||||||||||||
Medical condition: Small intestinal bacterial overgrowth (SIBO) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006887-44 | Sponsor Protocol Number: RGHT000396 | Start Date*: 2007-06-19 | |||||||||||
Sponsor Name:Royal Group Hospitals Trust | |||||||||||||
Full Title: Non-invasive bed-side measurement of systemic endothelial function in patients undergoing abdominal aortic aneurysm repair; modulation by ascorbic acid | |||||||||||||
Medical condition: Abdominal Aortic Aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009096-35 | Sponsor Protocol Number: QGUY/2008/TA-270/-01 | Start Date*: 2009-03-12 | |||||||||||
Sponsor Name:Activus Pharma Co., Ltd | |||||||||||||
Full Title: An open-label, 28-day multiple dose pilot study to evaluate the effects on lung oxidative stress, safety and pharmacokinetics of TA-270 in patients with chronic obstructive pulmonary disease (COPD). | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease. ( COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001676-38 | Sponsor Protocol Number: D1532C00079 | Start Date*: 2013-09-12 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase III, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy and Safety of Selumetinib (AZD6244; ARRY-142886) (Hyd-Sulfate) in Combination with Docetaxel, in Patients rece... | ||
Medical condition: Locally Advanced or Metastatic Non Small Cell Lung Cancer stage IIIb - IV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Ongoing) GB (GB - no longer in EU/EEA) IT (Ongoing) DE (Completed) NL (Ongoing) AT (Completed) ES (Temporarily Halted) BE (Ongoing) SE (Completed) PL (Completed) PT (Temporarily Halted) FR (Ongoing) BG (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000533-31 | Sponsor Protocol Number: 17GA001 | Start Date*: 2017-11-07 | ||||||||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | ||||||||||||||||||
Full Title: TReatment of Irritable bowel syndrome using Titrated ONdansetron Trial | ||||||||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhoea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004127-38 | Sponsor Protocol Number: TILATT/0708 | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: USE OF ORAL TILACTASE ENZYMES IN SUBJECTS WITH LACTOSE MALABSORPTION AND INTOLERANCE. CLINICAL RELEVANCE IN A POPULATION WITH HIGH PREVALENCE OF LACTASE DEFICIENCY IN SOUTHERN ITALY. | |||||||||||||
Medical condition: primary lactase deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004934-42 | Sponsor Protocol Number: PM L 0161 | Start Date*: 2006-04-13 | |||||||||||
Sponsor Name:SANOFI-AVENTIS OTC | |||||||||||||
Full Title: Efficacy evaluation of Enterogermina, 2 billion Bacillus clausii spores, on eradication of small intestinal bacterial overgrowth a randomised, parallel-group, open study | |||||||||||||
Medical condition: irritable bowel syndrome according to Rome II criteria and small intestinal bacterial overgrowth | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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