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ESTxENDS Trial- Substudy on Oxidative Stress Induced by Electronic Nicotine Delivery Systems (ENDS) Measured in EBC

Not Applicable
Completed
Conditions
Smoking Cessation
Oxidative Stress
Interventions
Other: ENDS (vaporizer/e-cig) and smoking cessation counseling
Other: Smoking cessation counseling
Registration Number
NCT03612453
Lead Sponsor
University of Bern
Brief Summary

--\> This is a substudy of the main ESTxENDS trial (NCT03589989). Oxidative stress outcomes should be considered secondary outcomes of the main smoking cessation outcome formulated in NCT03589989.

Cigarette smoking is the leading cause of preventable death in Switzerland and still more than a quarter of the Swiss population smokes cigarettes. Recently, electronic nicotine delivery systems (ENDS; also called vaporizer or electronic cigarette) have become popular with smokers who want to stop smoking or reduce their exposure to inhaled chemicals since ENDS use appears to be safer than tobacco smoking.

Smoking induces inflammation leading to acute and chronic oxidative stress, both evidenced in in vitro and in vivo studies. Tobacco-smoke contains free reactive radicals that generate reactive oxygen species (ROS). Afterwards ROS in turn induce oxidative stress, which likely plays a key role in causing airways and related pathologies linked to tobacco-smoke exposure. Acute and chronic oxidative stress can be measured by quantifying two biomarkers in exhaled breath condensates: 8-iso-prostaglandin F2α (8-isoprostane) and 8-Oxo-2'-deoxyguanosine (8-OHdG). 8-isoprostane, a marker of lipoperoxidation, results mainly from the non-enzymatic action of free radical attack on arachidonic fatty acids. 8-OHdG is a marker of DNA oxidation caused by ROS, and a predictor of lung cancer.

Oxidative stress between smokers who quit (with or without ENDS) and those who use ENDS for a long time have not yet been assessed in the setting of a randomized controlled trial (RCT). This study will therefore test the efficacy of ENDS for cigarette smoking cessation, the safety of ENDS on adverse events, the exposure to inhaled chemicals and the effect of ENDS on health-related outcomes, in particular by measuring oxidative stress in exhaled breath condensates (EBC).

For the main ESTxENDS trial (NCT03589989), cigarette smokers motivated to quit smoking cigarettes will be included. Participants in the intervention group will receive an ENDS and nicotine-containing e-liquids, which they will be allowed to use ad libitum. Additionally, they will receive smoking cessation counseling. Participants in the control group will receive smoking cessation counseling only. All participants will be followed over a 6-month period. Measures of oxidative stress by means of exhaled breath condensates and urine samples will be assessed at baseline and at 6- months' follow-up by asking to breathe for 20 minutes in a vial kept frozen at -10°C to collect around 2 mL of EBC.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
155
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupENDS (vaporizer/e-cig) and smoking cessation counseling-
Control groupSmoking cessation counseling-
Primary Outcome Measures
NameTimeMethod
Oxidative stress assessment (8-isoprostane)6 months post quit date

Oxidative stress assessed by 8-isoprostane concentrations in exhaled breath condensate (EBC)

Oxidative stress assessment (8-OHdG)6 months post quit date

Oxidative stress assessed by 8-OHdG in exhaled breath condensate (EBC)

Secondary Outcome Measures
NameTimeMethod
Change in oxidative stress (8-isoprostane)Change from baseline to 6 months post quit date

Change in oxidative stress assessed by measuring 8-isoprostane in exhaled breath condensate (EBC)

Change in oxidative stress (8-OHdG)Change from baseline to 6 months post quit date

Change in oxidative stress assessed by measuring 8-OHdG in exhaled breath condensate (EBC)

Trial Locations

Locations (1)

Unisanté, Centre universitaire de médecine générale et santé publique, Université de Lausanne

🇨🇭

Lausanne, Vaud, Switzerland

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