Nicotine Replacement Therapy and Cardiovascular Disease

Smoking Cessation Clinical Trial

Official title:

A Retrospective, Real-life Evaluation of the Cardiovascular Disease Risk Associated With Exposure to Pharmacological Smoking Cessation Interventions in a Representative UK Primary Care Patient Population.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02195739
• Other study ID #: E02311
• Status: Active, not recruiting
• Phase: N/A
• First received: May 14, 2014
• Last updated: September 30, 2014
• Start date: September 2013
• Est. completion date: December 2014

Study information

• Verified date: September 2014
• Source: Research in Real-Life Ltd
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Observational

Clinical Trial Summary

The aim of this study is to compare the cardiovascular disease event rate in smokers undertaking pharmacologically unaided smoking cessation attempts (the non-exposed group) with the event rate in smokers attempting smoking cessation assisted by pharmacological interventions - by nicotine replacement therapy (as any, or a combination, of: nasal spray, transdermal patches, inhaler or gum and tablets) or other pharmacological smoking cessation aids (e.g. bupropion [Zyban®] and varenicline [Champix®]) - in a representative UK primary care population.

Description:

Preliminary study data have indicated a possible increased cardiovascular disease risk in patients exposed to nicotine replacement therapy compared with controls (i.e. non-nicotine replacement therapy exposed patients) of a magnitude that could not reasonably be accounted for by differences in the cardiovascular risk profile of the two patient groups. Further in-depth studies in this area are warranted.

This retrospective study will compare the cardiovascular disease event risk in a group of smokers undertaking pharmacologically unaided smoking cessation attempts with the event rate in a group of smokers attempting smoking cessation assisted by pharmacological interventions (any of nicotine replacement therapy, bupropion or varenicline) in a representative UK primary care population.

There are three main types of pharmacological interventions currently available for smoking cessation, each of which has demonstrated efficacy when used in conjunction with behavioural support: nicotine replacement therapy, bupropion, and varenicline. Other medications, especially nortryptiline and clonidine, are considered to be effective adjunct therapy in smoking cessation, but they remain second-line options at this time.

Nicotine replacement therapy has been available since the 1980s and bupropion since 2000. Either approach to cessation doubles the chance of achieving abstinence when compared with unsupported quit attempts. After being granted its European licence in 2006, varenicline joined the pharmacological smoking cessation armamentarium. It is the first drug developed specifically for the treatment of tobacco dependence that contains no nicotine, and it triples smokers' chances of quitting compared with unsupported quit attempts.

As the fore-runner, nicotine replacement therapy is the longest-standing of the existing pharmacological smoking cessation interventions currently available. It aims to alleviate nicotine withdrawal symptoms by substituting the nicotine attained through tobacco smoking via alternative means (e.g. nasal sprays, inhalers, gum and tablets, transdermal patches). The various nicotine replacement therapy products available have differing durations of action and allow patients to tailor their nicotine intake according to their particular needs.For example, patches can be used to substitute for background nicotine and gums or tablets can be used to help satisfy urges.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 61050
• Est. completion date: December 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• The analysis will include an exposure group comprising smokers with no recorded smoking cessation attempts using pharmacological aids in the prior year, whose first recorded smoking cessation intervention was a cessation attempt assisted by either nicotine replacement therapy (using any of, or a combination of products) or another pharmacological smoking cessation intervention (e.g. bupropion, varenicline) at the index date.

Patients must also meet the following inclusion criteria:

• Aged: 18-75 years.

• Have at least one year of up-to-standard baseline data as defined by Clinical Practice Research Datalink (prior to the index smoking cessation attempt) and at least one year of up-to-standard outcome data (following the index smoking cessation attempt) or up-to-standard data up to the time of death if death occurred within the outcome period.

Exclusion Criteria:

Patients will be excluded from the analysis if they:

• Have had exposure to any nicotine replacement therapy or other pharmacological smoking cessation interventions in the baseline period (year prior to the index smoking cessation attempt), and/or

• Switched between types of smoking cessation interventions (i.e. nicotine replacement therapy to other pharmacological smoking cessation interventions or vice versa) during the outcome period(s). Switching between different nicotine replacement therapy products, or use of multiple nicotine replacement therapy products, will be permissible and analysis may involve a comparison of outcomes relative to nicotine exposure over the various outcome periods.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Cardiovascular Diseases
• Smoking Cessation

Locations

Country	Name	City	State
United Kingdom	Research in Real Life Ltd	Cambridge

Sponsors (1)

Lead Sponsor	Collaborator
Research in Real-Life Ltd

Country where clinical trial is conducted

United Kingdom, 

References & Publications (6)

British Medical Association and the Royal Pharmaceutical Society of Great Britain. British National Formulary. Version 56. London; BNF Group; 2008.

Cahill K, Stead LF, Lancaster T. Nicotine receptor partial agonists for smoking cessation. Cochrane Database Syst Rev. 2007 Jan 24;(1):CD006103. Review. Update in: Cochrane Database Syst Rev. 2008;(3):CD006103. — View Citation

Fiore MC, Bailey WC, Cohen SJ, et al. Treating tobacco use and dependence. Clinical practice guideline. Rockville (MD): US Department of Health and Human Services, Public Health Service, 2000

Le Foll B, George TP. Treatment of tobacco dependence: integrating recent progress into practice. CMAJ. 2007 Nov 20;177(11):1373-80. Review. Erratum in: CMAJ. 2008 Mar 11;178(6):732. — View Citation

Stead LF, Perera R, Bullen C, Mant D, Lancaster T. Nicotine replacement therapy for smoking cessation. Cochrane Database Syst Rev. 2008 Jan 23;(1):CD000146. doi: 10.1002/14651858.CD000146.pub3. Review. Update in: Cochrane Database Syst Rev. 2012;11:CD000146. — View Citation

West R, McNeill A, Raw M. Smoking cessation guidelines for health professionals: an update. Health Education Authority. Thorax. 2000 Dec;55(12):987-99. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Survival time for coronary heart disease-related death	Analysed using Cox's proportional hazards model.	Any time after index smoking cessation attempt	No
Other	Survival time for cerebrovascular disease-related death	Analysed using Cox's proportional hazards model.	Any time after index smoking cessation attempt	No
Other	Survival time for all-cause mortality	Analysed using Cox's proportional hazards model.	Any time after index smoking cessation attempt	No
Primary	Time to first coronary heart disease diagnosis	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt. Excluding patients with prior coronary heart disease.	4 weeks	No
Primary	Time to first cerebrovascular disease diagnosis.	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt. Excluding patients with prior cerebrovascular disease.	4 weeks	No
Secondary	Time to first coronary heart disease diagnosis	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt. Excluding patients with prior coronary heart disease.	52 weeks	No
Secondary	Time to first cerebrovascular disease diagnosis	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt. Excluding patients with prior cerebrovascular disease.	52 weeks	No
Secondary	Odds of recording one or more consultations for coronary heart disease or cerebrovascular disease	Analysed using conditional logistic regression model. Recorded General Practice consultations or hospital attendances for coronary heart disease or cerebrovascular disease, including General Practice consultations, Accident & Emergency attendance, out-patient department attendance or in-patient admissions.	52 weeks	No
Secondary	Survival time for coronary heart disease-related death.	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt.	52 weeks	No
Secondary	Survival time for cerebrovascular disease-related death.	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt.	52 weeks	No
Secondary	Survival time for all-cause mortality.	Analysed using Cox's proportional hazards model. Time from index smoking cessation attempt.	52 weeks	No

External Links

•   eto R, Lopez AD, Boreham J, et al. 2006. Mortality from smoking in developed countries 1950 - 2000 (2nd ed.) [online]
•   World Health Organization (WHO). 2007. The European tobacco control report 2007 [online]