Efficacy of Nicotine in Preventing COVID-19 Infection

Last updated: February 15, 2021
Sponsor: Assistance Publique - Hôpitaux de Paris
Overall Status: Active - Recruiting

Phase

3

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT04583410
APHP200538
2020-003722-23
  • Ages > 18
  • All Genders

Study Summary

The coronavirus disease (COVID-19) epidemic represents a major therapeutic challenge. The highly contagious severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) and the long duration of the disease have led to a massive influx of patients admitted in health services and intensive care units.

According to current knowledge, there are no treatments that prevent the spread of the infection, especially in exposed populations, or the disease progression to a severe form.

Daily active smokers are infrequent among outpatients or hospitalized patients with COVID-19. Several arguments suggest that nicotine is responsible for this protective effect via the nicotinic acetylcholine receptor (nAChR).

Nicotine may inhibit the penetration and spread of the virus and have a prophylactic effect in COVID-19 infection.

However, the epidemic is progressing throughout French territory and new variants (in particular the "English B1. 1.7 variant of SARS-COV-2") much more contagious run a risk of accelerating the epidemic in the population. The anti-SARS-COV-2 vaccines recently launched (or being evaluated) represent great hope in this health crisis, but trials were only able to show their effectiveness on symptomatic forms of SARS-COV-2 infection. On the one hand, the vaccination compaign for the entire population requires many months,which leaves many unprotected subjects waiting. In addition, there is currently no evidence of a protective role of vaccines against asymptomatic forms of COVID-19 and therefore on SARS-COV-2 transmission. Finally, the nicotine patches may protect people in hight-risk areas/periods until they are vaccinated (if they accept it and are eligible for it) and in the post-vaccination weeks necessary for the effectiveness of the vaccine,which reinforces the importance of evaluating this alternative prevention strategy, in the context of the arrival of vaccines

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Aged 18 or over
  2. May be followed for the duration of the study
  3. Obtaining free, informed and signed consent
  4. Affiliated to a social security scheme or beneficiary of such a scheme (except AME)
  5. Non-smoker and non-vaping (for former smokers or vapers: abstinent for at least 12months)

Exclusion

Exclusion Criteria:

  1. Symptoms suggestive of COVID-19 on the day of inclusion or in the past 14 days
  2. Documented history of COVID-19 and / or positive SARS-COV2 serology before the day ofinclusion
  3. Treatment ongoing with nicotine replacement therapy, varenicline or bupropion within 30 days before inclusion
  4. Known addiction problem to alcohol (defined by AUDIT-C > or = 10) or other substances.
  5. Vaccinated against COVID19 infection.
  6. Contraindications for nicotine patches:
  • pregnant woman (negative pregnancy test on inclusion) or breastfeeding woman
  • lack of effective contraception for women of childbearing potential
  • Generalized skin conditions that can interfere with the use of a transdermalpatch
  • stroke or myocardial infarction or acute coronary syndrome for less than 3 months
  • allergy to nicotine or to one of the excipients of the transdermal patch
  • Uncontrolled high blood pressure
  • Unstable or worsening angor
  • Severe cardiac arrhythmia (defined by wearing an automatic implantabledefibrillator)
  • Obliterating peripheral arterial disease
  • Known severe heart failure
  • Known severe renal or hepatic impairment,
  • Pheochromocytoma
  • Uncontrolled hyperthyroidism
  • Esophagitis due to gastroesophageal reflux disease or active peptic ulcer 7 Already included in an interventional trial evaluating a health product 8 Staffunder guardianship or curatorship or deprived of their liberty by a judicial oradministrative decision 9 Do not have a smartphone

Study Design

Total Participants: 1633
Study Start date:
October 22, 2020
Estimated Completion Date:
June 30, 2022

Connect with a study center

  • Centre Hospitalier Gonesse

    Gonesse, 95500
    France

    Active - Recruiting

  • Groupe Hospitalier de la Région de Mulhouse Sud Alsace

    Mulhouse, 68100
    France

    Site Not Available

  • Hôpital Pitié Salpêtrière - Service de Médecine Interne

    Paris, 75013
    France

    Active - Recruiting

  • Hôpital Sainte-Anne

    Paris, 75014
    France

    Site Not Available

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