- Trials with a EudraCT protocol (117)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
117 result(s) found for: Breath analysis.
Displaying page 1 of 6.
EudraCT Number: 2018-002579-16 | Sponsor Protocol Number: CF001 | Start Date*: 2018-08-26 | |||||||||||
Sponsor Name:Karolinska University Hospital, Stockholm CF center | |||||||||||||
Full Title: Evaluation of the possible use of analysis of posaconazole in exhaled breath as a surrogate marker for the lung to monitor adequate dosages of posaconazole in CF patients treated for Aspergillus sp... | |||||||||||||
Medical condition: Cystic Fibrosis (CF) is the most common life–limiting autosomal recessive disease among people of European heritage. The condition is a result of a mutation in the cystic fibrosis transmembrane con... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005411-16 | Sponsor Protocol Number: NASH-EX-1114 | Start Date*: 2015-06-30 |
Sponsor Name:Exalenz Bioscience Ltd. | ||
Full Title: Clinical Study of the BreathID® System to train the algorithm for the 13C-Octanoate Breath Test with or without the 13C-Methacetin Breath Test (OBT and MBT respectively) for correlation with histol... | ||
Medical condition: Patients with Non-Alcoholic Fatty Liver Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Ongoing) BE (Completed) | ||
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 (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000982-30 | Sponsor Protocol Number: 4993/15 | Start Date*: 2016-08-08 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Personalized pharmacological treatment of chronic obstructive pulmonary disease based on phenotyping: interventional study | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000891-17 | Sponsor Protocol Number: 221 | Start Date*: 2010-03-26 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Biosensors in the exhaled breath analysis comparison between healthy and asthmatic children and effect of montelukast and fluticasone on frequency pattern detected by biosensors in children with ... | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000890-51 | Sponsor Protocol Number: 200 | Start Date*: 2007-03-13 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Biosensors in the exhaled breath analysis: comparison between healthy and asthmatic adults and effect of montelukast and fluticasone on frequency pattern detected by biosensors in adults with asthma | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003722-33 | Sponsor Protocol Number: REROS/001/17 | Start Date*: 2018-03-02 | |||||||||||
Sponsor Name:ALFASIGMA S.P.A. | |||||||||||||
Full Title: Safety and Efficacy of Rifaximin Delayed Release 400 mg Tablets in Patients with Moderate-to-Severe Papulopustular Rosacea and Positive Lactulose Breath Test. A Multicenter Double-Blind, Placebo-Co... | |||||||||||||
Medical condition: Moderate-to-Severe Papulopustular Rosacea and Positive Lactulose Breath Test | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003501-10 | Sponsor Protocol Number: MBWtodetectPEXinCF | Start Date*: 2020-04-08 |
Sponsor Name:Västra Götalandsregionen | ||
Full Title: Use of repeated Multiple Breath Washout to detect and treat pulmonary exacerbation in children with Cystic Fibrosis, a multicenter randomized controlled study. | ||
Medical condition: Cystic fibrosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) DK (Prematurely Ended) NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003564-31 | Sponsor Protocol Number: 190580-001 | Start Date*: 2020-01-16 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Low dose catheter directed thrombolysis for acute intermediary-high risk pulmonary embolism. | |||||||||||||
Medical condition: Acute intermediary-high risk pulmonary embolism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003971-20 | Sponsor Protocol Number: CE01-300 | Start Date*: 2013-05-07 | |||||||||||
Sponsor Name:Cempra Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Oral Solithromycin (CEM-101) Compared to Oral Moxifloxacin in the Treatment of Adult Patients with Community-Ac... | |||||||||||||
Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) PL (Completed) LV (Completed) EE (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005544-10 | Sponsor Protocol Number: NIHRCDF | Start Date*: 2012-04-10 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Improving Inhaler Treatment and Small Airways Assessment in Chronic Obstructive Pulmonary Disease | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023366-49 | Sponsor Protocol Number: Bosentan for HPS | Start Date*: 2011-07-22 |
Sponsor Name:Med. Univ. Wien, Univ. Klinikum für Interne Medizin III | ||
Full Title: Bosentan for treatment ofhepatopulmonary syndrome in patients with liver cirrhosis - a prospective double blind randomized controlled clinical study | ||
Medical condition: HPS is by far the most frequent respiratory complication of cirrhosis leading to significantly increased mortality. The only therapeutic option is liver transplantation. Many patients with HPS who ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-007226-19 | Sponsor Protocol Number: TZP-102-CL-G002 | Start Date*: 2009-05-15 | |||||||||||
Sponsor Name:Tranzyme Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Evaluation of the Safety and Efficacy of Once-Daily Administrations of TZP 102 for the Treatment of Symptomatic... | |||||||||||||
Medical condition: The medical condition to be investigated is gastroparesis due to diabetes mellitus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000851-15 | Sponsor Protocol Number: UoB1581 | Start Date*: 2012-10-25 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: What is the clinical and cost effectiveness of oral steroids in the treatment of acute lower respiratory tract infection (LRTI)? A placebo controlled randomised trial | |||||||||||||
Medical condition: Acute lower respiratory tract infection/bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002605-10 | Sponsor Protocol Number: CJDQ443B12301 | Start Date*: 2022-04-01 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: KontRASt-02: A randomized, controlled, open label, phase III study evaluating the efficacy and safety of JDQ443 versus docetaxel in previously treated subjects with locally advanced or metastatic K... | |||||||||||||
Medical condition: Advanced non-small cell lung cancer harboring the KRAS G12C mutation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BG (Completed) HU (Trial now transitioned) ES (Ongoing) NO (Completed) GR (Trial now transitioned) PT (Trial now transitioned) FI (Trial now transitioned) DK (Completed) SI (Trial now transitioned) EE (Completed) IT (Trial now transitioned) PL (Completed) HR (Completed) IS (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003453-13 | Sponsor Protocol Number: CE01-301 | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Cempra Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Intravenous to Oral Solithromycin (CEM-101) Compared to Intravenous to Oral Moxifloxacin in the Treatment of Ad... | |||||||||||||
Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) LV (Completed) DE (Completed) ES (Completed) RO (Completed) SK (Completed) NL (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005080-33 | Sponsor Protocol Number: FARM7K7XZB | Start Date*: 2009-02-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA VINCENZO MONALDI DI NAPOLI | |||||||||||||
Full Title: RANDOMIZED, SINGLE BLIND, CONTROLLED TRIAL OF INHALED GLUTATHIONE VERSUS PLACEBO IN PATIENTS WITH CYSTIC FIBROSIS. | |||||||||||||
Medical condition: Cystic fibrosis. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012141-34 | Sponsor Protocol Number: ORTH-016 | Start Date*: 2009-06-29 |
Sponsor Name:University Hospital of North Tees and Hartlepool | ||
Full Title: Randomised Controlled Trial of the Use of Topical Application of Tranexamic Acid in Primary Total Hip Replacement. | ||
Medical condition: Blood loss in total hip replacement in patient with ostoearthritis and rheumatoid arthritis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000057-27 | Sponsor Protocol Number: 72544 | Start Date*: 2021-10-27 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Recovery of carotid body function after full recovery neuromuscular block | ||
Medical condition: Postoperative ventilatory control | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001438-34 | Sponsor Protocol Number: 20-101 | Start Date*: 2005-05-23 |
Sponsor Name:McNeil Consumer and Specialty Pharmaceuticals | ||
Full Title: A Phase II, Randomized, Investigator-Blinded, Parallel-Group, Pilot Study Evaluating the Safety, Palatability and Efficacy of Four Doses of Pancrelipase Microtablets in the Treatment of Infants and... | ||
Medical condition: Cystic Fibrosis-Related Pancreatic Insufficiency and Fat Malabsorption | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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