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Efficacy of Nicotine in Preventing COVID-19 Infection (NICOVID-PREV)

Primary Purpose

Covid19, SARS-Associated Coronavirus as Cause of Disease Classified Elsewhere

Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Nicotine patch
Placebo patch
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring Covid19, SARS-COV2, Preventing infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 12 months)

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 of inclusion
  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 transdermal patch
    • 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 implantable defibrillator)
    • 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 Staff under guardianship or curatorship or deprived of their liberty by a judicial or administrative decision 9 Do not have a smartphone

Sites / Locations

  • Centre Hospitalier GonesseRecruiting
  • Groupe Hospitalier de la Région de Mulhouse Sud Alsace
  • Hôpital Pitié Salpêtrière - Service de Médecine InterneRecruiting
  • Hôpital Sainte-Anne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Nicotine patch

Placebo patch

Arm Description

Outcomes

Primary Outcome Measures

SARS-COV2 seroconversion between W0 and W19 after randomization
This is the proportion of subjects with at least one positive serology between W2 and W19. The time of S19 takes into account a seroconversion delay of 5 weeks in relation to the SARS-CoV2 contamination.

Secondary Outcome Measures

Proportion of documented symptomatic COVID-19 infection
SARS-COV2 seroconversion
This is the proportion of patients with at least one positive serology between W2 and W16.
Asymptomatic COVID-19 infection proportion at week 14
Asymptomatic COVID-19 infection is defined as SARS-CoV2 seroconversion at Week 19 without symptoms suggestive of COVID until the end of Week 16 to take in account of the two weeks of incubation period
Proportion of severe COVID-19 infection
documented infection (positive SARS-CoV2 PCR test and / or suggestive chest CT scan and / or seroconversion) whose first symptoms appeared before W8 and W16 respectively, and requiring hospitalization or home oxygen therapy, or having resulted in death
Number of sick leaves for a COVID-19 infection
Number of days off during sick leaves for a COVID-19 infection
Proportion of AE, SAE
Intensity and frequency of nausea, dizziness, feeling of empty head, headache, vomiting
Proportion of active smoker or active vapers or taking nicotine substitutes documented by examination
Proportion of active smoker or active vapers or taking nicotine substitutes documented by urinary cotinine
Mean score of Desire to smoke defined by French Tobacco Craving scale
Mean score of Withdrawal symptoms scale
Dosage of cotinine in the urine
Mean score of Fatigue Numeric rating scale
Weight
Mean score of Hospital anxiety and depression scale
Mean score of Insomnia severity scale
Positive and negative syndrome scale

Full Information

First Posted
September 28, 2020
Last Updated
February 15, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT04583410
Brief Title
Efficacy of Nicotine in Preventing COVID-19 Infection
Acronym
NICOVID-PREV
Official Title
Efficacy of Nicotine in Preventing COVID-19 Infection
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 22, 2020 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
June 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, SARS-Associated Coronavirus as Cause of Disease Classified Elsewhere
Keywords
Covid19, SARS-COV2, Preventing infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
1633 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nicotine patch
Arm Type
Experimental
Arm Title
Placebo patch
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Nicotine patch
Intervention Description
NICOPATCHLIB, 7mg/24h Day 1 to day 3 : 3,5 mg/day Day 4 to day 9 : 7 mg/day Day 10 to Day 15 : 10,5 mg/day Day 16 to day 98 : 14 mg/day Decrease treatment Day 99 to day 105 : 10,5 mg/day Day 106 to day 112 : 7 mg/day Day 113 to Day 119 : 3,5 mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo patch
Intervention Description
PLACEBO OF NICOPATCHLIB, 7mg/24h Day 1 to day 3 : 3,5 mg/day Day 4 to day 9 : 7 mg/day Day 10 to Day 15 : 10,5 mg/day Day 16 to day 98 : 14 mg/day Decrease treatment Day 99 to day 105 : 10,5 mg/day Day 106 to day 112 : 7 mg/day Day 113 to Day 119 : 3,5 mg/day
Primary Outcome Measure Information:
Title
SARS-COV2 seroconversion between W0 and W19 after randomization
Description
This is the proportion of subjects with at least one positive serology between W2 and W19. The time of S19 takes into account a seroconversion delay of 5 weeks in relation to the SARS-CoV2 contamination.
Time Frame
Between week 0 and week 19
Secondary Outcome Measure Information:
Title
Proportion of documented symptomatic COVID-19 infection
Time Frame
Week 8, Week16
Title
SARS-COV2 seroconversion
Description
This is the proportion of patients with at least one positive serology between W2 and W16.
Time Frame
Week 16
Title
Asymptomatic COVID-19 infection proportion at week 14
Description
Asymptomatic COVID-19 infection is defined as SARS-CoV2 seroconversion at Week 19 without symptoms suggestive of COVID until the end of Week 16 to take in account of the two weeks of incubation period
Time Frame
Week 14
Title
Proportion of severe COVID-19 infection
Description
documented infection (positive SARS-CoV2 PCR test and / or suggestive chest CT scan and / or seroconversion) whose first symptoms appeared before W8 and W16 respectively, and requiring hospitalization or home oxygen therapy, or having resulted in death
Time Frame
Week 8, Week16
Title
Number of sick leaves for a COVID-19 infection
Time Frame
Week 16
Title
Number of days off during sick leaves for a COVID-19 infection
Time Frame
Week 16
Title
Proportion of AE, SAE
Time Frame
From inclusion and week 25
Title
Intensity and frequency of nausea, dizziness, feeling of empty head, headache, vomiting
Time Frame
Week 25
Title
Proportion of active smoker or active vapers or taking nicotine substitutes documented by examination
Time Frame
Week 25
Title
Proportion of active smoker or active vapers or taking nicotine substitutes documented by urinary cotinine
Time Frame
Week 25
Title
Mean score of Desire to smoke defined by French Tobacco Craving scale
Time Frame
Week 25
Title
Mean score of Withdrawal symptoms scale
Time Frame
Week 25
Title
Dosage of cotinine in the urine
Time Frame
Week 8 and 25
Title
Mean score of Fatigue Numeric rating scale
Time Frame
Week 2, week 8, week 16
Title
Weight
Time Frame
Week 8, week 16, week 25
Title
Mean score of Hospital anxiety and depression scale
Time Frame
Week 2, week 8, week 16
Title
Mean score of Insomnia severity scale
Time Frame
Week 2, week 8, week 16
Title
Positive and negative syndrome scale
Time Frame
Week 2, week 8, week 16

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 or over May be followed for the duration of the study Obtaining free, informed and signed consent Affiliated to a social security scheme or beneficiary of such a scheme (except AME) Non-smoker and non-vaping (for former smokers or vapers: abstinent for at least 12 months) Exclusion Criteria: Symptoms suggestive of COVID-19 on the day of inclusion or in the past 14 days Documented history of COVID-19 and / or positive SARS-COV2 serology before the day of inclusion Treatment ongoing with nicotine replacement therapy, varenicline or bupropion within 30 days before inclusion Known addiction problem to alcohol (defined by AUDIT-C > or = 10) or other substances. Vaccinated against COVID19 infection. 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 transdermal patch 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 implantable defibrillator) 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 Staff under guardianship or curatorship or deprived of their liberty by a judicial or administrative decision 9 Do not have a smartphone
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zahir AMOURA, MD
Phone
+33142178244
Email
zahir.amoura@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Florence TUBACH, MD
Email
florence.tubach@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zahir AMOURA, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Gonesse
City
Gonesse
ZIP/Postal Code
95500
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Isabelle AMOURA, MD
Email
isabelle.amoura@ch-gonesse.fr
Facility Name
Groupe Hospitalier de la Région de Mulhouse Sud Alsace
City
Mulhouse
ZIP/Postal Code
68100
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guylaine LABRO, MD
Email
guylaine.labro@ghrmsa.fr
Facility Name
Hôpital Pitié Salpêtrière - Service de Médecine Interne
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zahir AMOURA, MD
Email
zahir.amoura@aphp.fr
Facility Name
Hôpital Sainte-Anne
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raphael GAILLARD, MD
Email
r.gaillard@ghu-paris.fr

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Nicotine in Preventing COVID-19 Infection

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