Trial to Evaluate the Efficacy of Simvastatin for Smoking Cessation

NCT ID: NCT02399709

Last Updated: 2020-04-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 124 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-04-01
• Study Completion Date: 2017-11-03

Brief Summary

Tobacco smoking is the number one preventable cause of disease worldwide. Unfortunately, there are few smoking cessation agents and their effectiveness has been shown to be relatively limited and is associated with potential unwanted effects. Therefore, the discovery of new medications that can facilitate abstinence and reduce relapse to cigarette use represents a pressing necessity. In the attempt to find molecules that could reduce drug-seeking behavior, we discovered that simvastatin reduces cocaine and nicotine, but not food, seeking behavior in rats. This discovery of a new therapeutic application for an already marketed class of compounds may greatly facilitate the translation from preclinical to clinical setting. In this project, we aim at investigating whether simvastatin is an effective smoking cessation agent in humans.

The study design is a multicenter, randomized, double blind 2 parallel groups, clinical trial with an intention-to-treat analysis. Smokers will randomly be assigned to receive simvastatin or placebo for 3 months. 200 smokers (100 receiving simvastatin and 100 receiving placebo) will be recruited through already established networks of general practitioners. The primary outcome of the efficacy of simvastatin will be the rate of smoking abstinence during the last month of the 3-month treatment period, defined as reported continuous abstinence from smoking and confirmed by expired air carbon monoxide and urinary cotinine concentration. The last assessment will be done 6 months after the predefined quit date.

The results of this proof-of-concept study may open new perspectives in the treatment of tobacco use and dependance.

Conditions

Smoking Cessation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

simvastatin

oral administration, capsule of 20mg.

Group Type: EXPERIMENTAL

simvastatin

Intervention Type: DRUG

microcrystalline cellulose

oral administration, capsule of 20mg

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Interventions

simvastatin

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age >=18 and <=70 years,
• Smoking more than 10 cigarettes per day for at least 1 year,
• Motivated to quit smoking,
• Without legal tutors or subordination,
• Affiliated to a health insurance system as required by the French law on biomedical research,
• Written informed consent for participation in the study.

Exclusion Criteria

• Age < 18 or > 70 years,
• Presenting a contraindication to simvastatin use,
• With depression and/or psychosis and/or cognitive disorder and/or mental retardation or chronic use of medications for these disorders,
• Substance use disorder other than smoking,
• More than 3 months of abstinence from cigarette smoking in the previous year,
• Use of nicotine replacement therapy, bupropion, varenicline on last 3 months,
• Use of clonidine or nortriptyline on last 3 months,
• Undergoing on last 3 months' cognitive-behavioral therapy for smoking cessation,
• Premenopausal women without contraception.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Poitiers University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Marie-Christine PERAULT-POCHAT, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Poitiers University Hospital

Locations

Poitiers University Hospital

Poitiers, , France

Countries

France

Other Identifiers

ADDICSTATINE

Identifier Type: -

Identifier Source: org_study_id