- Trials with a EudraCT protocol (162)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
162 result(s) found for: Carbon monoxide.
Displaying page 1 of 9.
EudraCT Number: 2005-005678-61 | Sponsor Protocol Number: ESNOD-01 | Start Date*: 2006-02-22 |
Sponsor Name:University Hospital Tuebingen | ||
Full Title: Entwicklung einer Untersuchungsmethode zur Bestimmung des NO-Transferfaktors der Lunge Evaluierung der Methode und Normwerterhebung an gesunden Probanden (Development of a new method for steady-sta... | ||
Medical condition: Lung function testing (NO- and CO Transferfactor) in healthy subjects | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016446-50 | Sponsor Protocol Number: - | Start Date*: 2010-04-19 | |||||||||||
Sponsor Name:Maastricht University - CAPHRI School for Public Health and Primary Care | |||||||||||||
Full Title: Helping more smokers to quit by combining varenicline with counselling for smoking cessation. The COVACO randomized controlled trial. | |||||||||||||
Medical condition: Smoking: Subjects must be daily smokers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017599-26 | Sponsor Protocol Number: WS508648 | Start Date*: 2010-01-12 |
Sponsor Name:CENTRO PER LA PREVENZIONE E CURA DEL TABAGISMO | ||
Full Title: EFFICACY AND SAFETY OF SMOKING CESSATION WITH VARENICLINE TARTRATE IN DIBETIC SMOKERS: A DOUBLE-BLIND,PLACEBO-CONTROLLED, RANDOMIZED, TRIAL | ||
Medical condition: diabetic smokers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003250-29 | Sponsor Protocol Number: IPAB-07-002 | Start Date*: 2008-03-14 | |||||||||||
Sponsor Name:Independent Pharmaceutica AB | |||||||||||||
Full Title: A randomised, placebo-controlled, multi-centre study on the efficacy of Niccine, a vaccine for nicotine, in smoking relapse prevention, assessed in abstinent, adult smokers. | |||||||||||||
Medical condition: The intended indication for the drug under investigation is smoking relapse prevention. Tobacco smoking has been identified as the single largest preventable cause of morbidity and premature death ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001163-24 | Sponsor Protocol Number: GB28547 | Start Date*: 2013-11-04 |
Sponsor Name:F. Hoffmann-La Roche Ltd | ||
Full Title: A PHASE II, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, STUDY TO ASSESS THE EFFICACY AND SAFETY OF LEBRIKIZUMAB IN PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS. | ||
Medical condition: IDIOPATHIC PULMONARY FIBROSIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) ES (Completed) PL (Completed) GB (Completed) BE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021789-31 | Sponsor Protocol Number: A3051139 | Start Date*: 2010-12-08 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 US | |||||||||||||
Full Title: A PHASE 4 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY EVALUATING THE EFFICACY AND SAFETY OF RE-TREATMENT WITH VARENICLINE IN SUBJECTS WHO ARE CURRENTLY SMOKING, AND WHO HAVE PRE... | |||||||||||||
Medical condition: Smoking Cessation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005894-36 | Sponsor Protocol Number: ZonMw61200014/Nabi4508 | Start Date*: 2009-04-27 | |||||||||||
Sponsor Name:ZonMw [...] | |||||||||||||
Full Title: A Phase 2B, Multi-Center, Randomized, Double-Blinded, Parallel-Arm Study to Assess Efficacy and Safety of 3’-aminomethylnicotine-P. aeruginosa r-Exoprotein A Conjugate Vaccine (NicVAX®) or placebo,... | |||||||||||||
Medical condition: Smoking: Subjects must be smoking an average of at least 10 cigarettes per day during the past year and over the month prior to the screening visit, with no period of abstinence greater than 3 mont... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004978-42 | Sponsor Protocol Number: ADDICTSTATINE | Start Date*: 2015-02-25 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Pilot randomized double blind, placebo controlled trial of the efficacy of simvastatin for smoking cessation | |||||||||||||
Medical condition: Smoking cessation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001099-20 | Sponsor Protocol Number: CPR-EFC5515-EN-E02 | Start Date*: 2006-05-18 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: An international, seven-week, double blind, placebo-controlled, two parallel group study to assess the efficacy of dianicline 40 mg bid as an aid to smoking cessation in cigarette smokers | |||||||||||||
Medical condition: Cigarette smokers willing to quit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) NO (Completed) DK (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020688-18 | Sponsor Protocol Number: CQAX576A2203 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multipledose, exploratory proof of concept study to assess the safety, tolerability, efficacy, pharmacodynamics and pharmacokinetics of QAX576 in pa... | |||||||||||||
Medical condition: Patients with rapidly progressive idiopathic pulmonary fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003158-18 | Sponsor Protocol Number: 203PF203 | Start Date*: 2018-09-12 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of BG00011 in Patients With Idiopathic Pulmonary Fibrosis | |||||||||||||
Medical condition: mild to moderate Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) GR (Completed) BE (Completed) ES (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000138-11 | Sponsor Protocol Number: PIPF-006 | Start Date*: 2006-05-23 |
Sponsor Name:InterMune, Inc. | ||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Phase 3 Study of the Safety and Efficacy of Pirfenidone in Patients with Idiophatic Pulmonary Fibrosis | ||
Medical condition: Idiophatic Pulmonary Fibrosis (IPF) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) DE (Completed) BE (Completed) CZ (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005334-21 | Sponsor Protocol Number: DRI6938 | Start Date*: 2007-03-21 | |||||||||||
Sponsor Name:sanofi-aventis recherche et developpement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel group, fixed-dose, 8-week treatment, multi-center trial evaluating the dose effect relationship for efficacy and the safety of 3 oral doses ... | |||||||||||||
Medical condition: Aid to smoking cessation in cigarette smokers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) BE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000371-26 | Sponsor Protocol Number: DFI12712 | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:Genzyme Corporation | |||||||||||||
Full Title: A Phase 2/3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Repeat Dose Study to Evaluate the Efficacy, Safety, Pharmacodynamics and Pharmacokinetics of olipudase alfa in Patients With... | |||||||||||||
Medical condition: Patients with acid sphingomyelinase deficiency (Niemann-Pick Type B disease) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) PT (Completed) ES (Ongoing) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001174-25 | Sponsor Protocol Number: NC501/SC01904 | Start Date*: Information not available in EudraCT |
Sponsor Name:Neurocure Ltd | ||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE THE EFFICACY, SAFETY AND TOLERABILITY OF A COMBINATION OF GALANTAMINE (AN ACETYLCHOLINESTERASE INHIBITOR) PLUS TRIMIPRAMINE IN SMOKING CESSATION | ||
Medical condition: Healthy subjects who are smokers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002621-46 | Sponsor Protocol Number: 20878 | Start Date*: 2005-06-27 |
Sponsor Name:University of Nottingham | ||
Full Title: Double-blind, randomised, placebo-controlled trial of nicotine replacement therapy in pregnancy | ||
Medical condition: Smoking during pregnancy Specifically smoking 5 or more cigarettes currently (i.e. whilst pregnant) and having smoked 10 or more cigarettes prior to pregnancy. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004461-34 | Sponsor Protocol Number: 1.0 | Start Date*: 2006-11-02 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Open label randomised trial of nicotine replacement therapy and oral smokeless tobacco (snus) in smoking cessation | |||||||||||||
Medical condition: Smoking cessation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004148-31 | Sponsor Protocol Number: PREDMETH_NL71782.078.19 | Start Date*: 2020-02-26 |
Sponsor Name:Erasmus Medisch Centrum Dept. of Pulmonology | ||
Full Title: The PREDMETH trial: Effectiveness of methotrexate versus prednisone as first-line therapy for pulmonary sarcoidosis – A randomized controlled trial | ||
Medical condition: pulmonary sarcoidosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000822-24 | Sponsor Protocol Number: VP-C21-005 | Start Date*: 2020-07-06 | |||||||||||
Sponsor Name:Vicore Pharma AB | |||||||||||||
Full Title: A Phase 2, Multi-Centre, Open-Label, Single-Arm Trial Investigating the Safety, Efficacy and Pharmacokinetics of C21 in Subjects with Idiopathic Pulmonary Fibrosis | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004626-10 | Sponsor Protocol Number: 10003 | Start Date*: 2006-03-16 |
Sponsor Name:Pulmonary Department, Gentofte Hospital | ||
Full Title: Smoking cessation by nurses with smokelesstobacco buccal tabltes, nicotine buccal tablets, nicotine patches with repeated thearapy every 6 months for 2 years | ||
Medical condition: Smopking (nicotine addiction/Tobacco addiction) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
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