- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Tobacco smoke.
Displaying page 1 of 2.
| EudraCT Number: 2022-002492-11 | Sponsor Protocol Number: PRECESTO | Start Date*: 2023-09-13 | |||||||||||
| Sponsor Name:NFL BIOSCIENCES SA | |||||||||||||
| Full Title: Phase II Study Assessing Efficacy and Safety of NFL-101 on Reduction of Reinforcing Properties of Cigarettes | |||||||||||||
| Medical condition: Tobacco addiction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022334-92 | Sponsor Protocol Number: qmul250510 | Start Date*: 2011-01-07 |
| Sponsor Name:Barts and the London School of Medicine and Dentistry, Queen Mary University of London | ||
| Full Title: Effects of a combination of varenicline and transdermal nicotine patch on post-quitting urges to smoke | ||
| Medical condition: Tobacco dependence (smoking cessation) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002203-40 | Sponsor Protocol Number: 07.0056 | Start Date*: 2007-10-03 | |||||||||||
| Sponsor Name:St. George's, University of London | |||||||||||||
| Full Title: Effect of hydrocortisone on desire to smoke and tobacco withdrawal symptoms | |||||||||||||
| Medical condition: Nicotine addiction; specifically, cortisol deficiency following smoking cessation. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001267-36 | Sponsor Protocol Number: CO-160310091324-SCCT | Start Date*: 2016-06-08 |
| Sponsor Name:McNeil AB | ||
| Full Title: PHARMACODYNAMIC EFFECTS OF NICOTINE MOUTH SPRAY AND CYTISINE TABLET. A STUDY IN HEALTHY SMOKERS. | ||
| Medical condition: Tobacco Dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022335-11 | Sponsor Protocol Number: qmul010610 | Start Date*: 2011-01-07 |
| Sponsor Name:Barts and the London School of Medicine and Dentistry, Queen Mary University of London | ||
| Full Title: Effects of a tailored dose of varenicline on post-quitting urges to smoke | ||
| Medical condition: Tobacco dependence (smoking cessation) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015870-36 | Sponsor Protocol Number: NICTDP2011 | Start Date*: 2009-12-22 |
| Sponsor Name:McNeil AB | ||
| Full Title: Nicotine pharmacodynamics with a new oral nicotine replacement product and NiQuitin Lozenge. A study in healthy smokers. | ||
| Medical condition: Tobacco dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-004720-24 | Sponsor Protocol Number: qmul120508 | Start Date*: 2009-03-27 | ||||||||||||||||
| Sponsor Name:Queen Mary and Westfield College, University of London | ||||||||||||||||||
| Full Title: Effects of an extended period of varenicline use prior to quitting smoking on post-quitting urges to smoke | ||||||||||||||||||
| Medical condition: Tobacco Dependence (Smoking Cessation) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-005363-34 | Sponsor Protocol Number: EC/2008/50/FAHS | Start Date*: 2009-03-10 | |||||||||||
| Sponsor Name:University of Surrey | |||||||||||||
| Full Title: Investigation to explore whether there is a synergistic effect between nicotine replacement therapy and guided bodyscanning on cigarette cravings and withdrawal symptoms in temporarily abstinent sm... | |||||||||||||
| Medical condition: Healthy volunteers who currently smoke 10 or more cigarettes per day, for the last 3 years. The trial intends to explore whether there is a synergistic effect between the relaxation technique of g... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001764-21 | Sponsor Protocol Number: MANS11 | Start Date*: 2011-05-19 | |||||||||||
| Sponsor Name:Magle AB | |||||||||||||
| Full Title: The effect of 6 weeks’ use of the Nicachet 4 mg nicotine powder in pouch on the oral mucosa. A short-term smoking cessation and tolerability study. | |||||||||||||
| Medical condition: Nicotine addiction | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023268-42 | Sponsor Protocol Number: NICTDP2012 | Start Date*: 2011-03-25 |
| Sponsor Name:McNeil AB | ||
| Full Title: NICOTINE PHARMACODYNAMICS WITH A NEW ORAL NICOTINE REPLACEMENT PRODUCT AND NICOTINE GUM 4 MG. A STUDY IN HEALTHY SMOKERS. | ||
| Medical condition: Tobacco Dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005565-20 | Sponsor Protocol Number: QMUL111111 | Start Date*: 2012-05-02 | |||||||||||
| Sponsor Name:QUEEN MARY, UNIVERSITY OF LONDON | |||||||||||||
| Full Title: Comparison of the effects of the electronic cigarette and nicotine inhalator on tobacco withdrawal symptoms over 24 hours of abstinence | |||||||||||||
| Medical condition: Nicotine withdrawal state | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002731-28 | Sponsor Protocol Number: P12-01/BP1.4979 | Start Date*: 2013-03-01 | |||||||||||
| Sponsor Name:Bioprojet | |||||||||||||
| Full Title: Randomized placebo controlled trial assessing the efficacy and safety of BP1.4979 in smoking cessation | |||||||||||||
| Medical condition: Smoking cessation | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004575-11 | Sponsor Protocol Number: A6431079 | Start Date*: 2005-01-27 |
| Sponsor Name:Pfizer Health AB | ||
| Full Title: PERCEPTION AND TOLERABILITY OF NICOTINE FILMS FOR USE IN THE MOUTH. A RANDOMIZED, CROSSOVER, PHASE-II, STUDY IN HEALTHY SMOKERS. | ||
| Medical condition: Tobacco dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (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: 2004-003016-30 | Sponsor Protocol Number: A6431076 | Start Date*: 2005-01-04 |
| Sponsor Name:Pfizer Health AB | ||
| Full Title: PHARMACOKINETICS OF NICOTINE FILM FOR USE IN THE MOUTH. A RANDOMIZED, CROSSOVER, PHASE-I, COMPARATIVE STUDY IN HEALTHY SMOKERS. | ||
| Medical condition: Tobacco dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001507-76 | Sponsor Protocol Number: BRONCHIOLE2017 | Start Date*: 2017-09-20 |
| Sponsor Name:Region Örebro län | ||
| Full Title: Beta-blockeRs tO patieNts with CHronIc Obstructive puLmonary diseasE (BRONCHIOLE) A pragmatic clinical trial with partial registry-based follow-up | ||
| Medical condition: Chronic Obstructive Pulmonary disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002796-41 | Sponsor Protocol Number: NICTDP0002 | Start Date*: 2011-09-29 |
| Sponsor Name:McNeil AB | ||
| Full Title: A PROOF OF CONCEPT WITH A NEW NICOTINE INHALER IN COMPARISON WITH NICOTINE INHALER 10 MG - AN EXPLORATORY STUDY IN ADULT HEALTHY SMOKERS | ||
| Medical condition: Tobacco Dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001237-65 | Sponsor Protocol Number: | Start Date*: 2017-06-29 | ||||||||||||||||
| Sponsor Name:Queen Mary University of London, Joint Research Management Office | ||||||||||||||||||
| Full Title: Helping Pregnant smokers quit: A multi-centre RCT of electronic cigarettes and nicotine patches | ||||||||||||||||||
| Medical condition: Tobacco dependence/smoking cessation | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-006845-13 | Sponsor Protocol Number: A6431111 | Start Date*: 2009-02-02 | |||||||||||||||||||||
| Sponsor Name:McNeil AB (Johnson & Johnson Consumer and Personal Products Worldwide, J&J CPPW) | |||||||||||||||||||||||
| Full Title: Efficacy and safety following use of a novel nicotine replacement therapy. A multicenter, randomized, double blind, placebo-controlled, parallel group, 52-week study in smokers motivated to quit. | |||||||||||||||||||||||
| Medical condition: For the treatment of tobacco dependence by relieving nicotine craving and withdrawal symptoms, thereby facilitating smoking cessation in smokers motivated to quit abruptly. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2005-000917-37 | Sponsor Protocol Number: A6431081 | Start Date*: 2005-06-02 |
| Sponsor Name:Pfizer Health AB | ||
| Full Title: Comparision of single-dose nicotine pharmacokinetics of three variants of nicotine oral drops 2 mg and of Nicorette Gum 2 mg in healthy smokers | ||
| Medical condition: Tobacco dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
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