- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Nicotine patches.
Displaying page 1 of 1.
EudraCT Number: 2008-006433-28 | Sponsor Protocol Number: RG_08_082_a02 | Start Date*: 2009-01-20 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||||||||||||
Full Title: Rapid reduction versus abrupt quitting for smokers who want to stop soon: a randomised controlled non-inferiority trial. | |||||||||||||||||||||||||||||||||
Medical condition: Smoking and nicotine addiction. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (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: 2007-006458-24 | Sponsor Protocol Number: V00116 TD 201 | Start Date*: 2008-01-23 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Analysis of the sensory profile of two new transdermal patches (V0116TD07AF019 and V0116TD07AF020) 21 mg/24h versus a reference transdermal patch (NICOTINELL TTS) 21 mg/24h. | |||||||||||||
Medical condition: Healthy volunteers, occasional or regular smokers. Intended indication: Relief of nicotine withdrawal symptoms, in nicotine dependency as an aid to smoking cessation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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: 2014-003720-43 | Sponsor Protocol Number: NIK-08-2014 | Start Date*: 2014-12-17 |
Sponsor Name:Fakultní nemocnice Ostrava | ||
Full Title: "Prevention of nicotine abstinence in critically ill patients after major surgery" | ||
Medical condition: Nicotin abstinence delirium | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004692-36 | Sponsor Protocol Number: VAR/01/011 | Start Date*: 2011-11-30 | ||||||||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | ||||||||||||||||||
Full Title: COMBIVAR. Randomized double-blind trial of two parallel groups design to evaluate the efficacy of smoking cessation with combined (varenicline plus nicotine patches) versus monotherapy (varenicline) | ||||||||||||||||||
Medical condition: NICOTINE DEPENDENCE. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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) |
EudraCT Number: 2004-002058-69 | Sponsor Protocol Number: UHL 9609 | Start Date*: 2004-11-17 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: The use of nicotine patches for the treatment of psoriasis | ||
Medical condition: Psoriasis - moderate to severe | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017862-22 | Sponsor Protocol Number: 200110005 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:ZonMw | |||||||||||||
Full Title: The effectiveness of Nicotine Replacement Therapy for young people aged 12 to 18 years | |||||||||||||
Medical condition: Smoking among young people aged 12 – 18 years. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003722-23 | Sponsor Protocol Number: APHP200538 | Start Date*: 2020-10-02 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Efficacy of nicotine in preventing COVID-19 infection | |||||||||||||
Medical condition: Hospital staff (medical and non-medical), with COVID19 negative diagnosis (SARS-CoV2 serology and SARS-Cov2 PCR) working in contact with COVID-19 positive patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020299-42 | Sponsor Protocol Number: KKS-135 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:Philipps-University Marburg | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, multi-center trial to assess the disease-modifying potential of transdermal nicotine in early Parkinson's disease in Germany and the USA (NIC-PD) | |||||||||||||
Medical condition: Early PD subjects within 18 months of diagnosis and not expected to require dopamine agonist or levodopa therapy for 1 year, with Hoehn and Yahr stage <2, with stable (>2 months) MAO-B inhibitor th... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005134-19 | Sponsor Protocol Number: RG_11-171 | Start Date*: 2012-01-31 |
Sponsor Name:University of Birmingham | ||
Full Title: An open label pragmatic randomised controlled trial of nicotine patch preloading for smoking cessation. | ||
Medical condition: The IMP will assist smoking cessation in smokers wishing to stop. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000106-24 | Sponsor Protocol Number: RAA2006/004 | Start Date*: 2006-06-26 |
Sponsor Name:Kings College London (IOP) | ||
Full Title: Using genotype to tailor prescribing of nicotine replacement therapy: a randomised controlled trial assessing impact upon adherence | ||
Medical condition: Smoking addiction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000369-37 | Sponsor Protocol Number: NKT102245 | Start Date*: 2005-02-01 |
Sponsor Name:GlaxoSmithKline Group of Companies | ||
Full Title: A multicentre, randomised, double-blind, placebo-controlled, parallel group study to evaluate the safety and efficacy of oral dosing with GW679769 (50 mg or 150 mg) for 3 consecutive days in conjun... | ||
Medical condition: Post Operative Nausea and Vomiting (PONV) Post Discharge Nausea and Vomiting (PDNV) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HU (Completed) GB (Completed) ES (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001021-22 | Sponsor Protocol Number: NKO101287 | Start Date*: 2005-02-08 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A Multicentre, Randomised, Double-blind, Double-dummy, Placebo-controlled, Parallel Group, Phase II Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Oral (25 mg) and Intravenous (3 m... | ||
Medical condition: Post Operative Nausea and Vomiting (PONV) Post Discharge Nausea and Vomiting (PDNV) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005284-16 | Sponsor Protocol Number: MK-8342B-072 | Start Date*: 2016-06-07 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase I, Open-Label Study to Investigate the Pharmacokinetics and Pharmacodynamics of Etonogestrel (ENG) and 17ß-Estradiol (E2) in Healthy female Postmenarcheal Adolescents and Healthy Female Adu... | |||||||||||||
Medical condition: Hormonal contraception and primary dysmenorrhea in woman seeking contraception. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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