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Oral adverse event reporting in smoking cessation trials using non-combustible nicotine products: A quality assessment

Authors
 Rosa, Giusy Rita Maria La  ;  Del Giovane, Cinzia  ;  Minozzi, Silvia  ;  Kowalski, Jan  ;  Chapple, Iain  ;  Amaliya, Amaliya  ;  Zakiawati, Dewi  ;  Ludovichetti, Francesco Saverio  ;  Il Kim, Baek  ;  Tilakaratne, Wanninayake Mudiyanselage  ;  Farsalinos, Konstantinos  ;  Polosa, Riccardo 
Citation
 JOURNAL OF DENTISTRY, Vol.162, 2025-11 
Article Number
 106057 
Journal Title
JOURNAL OF DENTISTRY
ISSN
 0300-5712 
Issue Date
2025-11
MeSH
Electronic Nicotine Delivery Systems ; Humans ; Nicotine* / adverse effects ; Randomized Controlled Trials as Topic* / standards ; Research Design / standards ; Smoking Cessation* / methods ; Tobacco Products* / adverse effects ; Tobacco Use Cessation Devices* / adverse effects ; Tobacco, Smokeless / adverse effects
Keywords
CONSORT harms ; E -cigarette ; Nicotine replacement therapy ; Non-combustible nicotine products ; Oral adverse events ; Snus ; Safety ; Smoking cessation
Abstract
Objectives: To assess the completeness and quality of reporting of oral adverse events (OAEs) in randomized controlled trials (RCTs) that evaluated non-combustible nicotine products (NCNPs) and whether reporting practices have improved over time. Data sources and study selection: This secondary data analysis was based on 36 RCTs included in a previous systematic review. Trials involved adult smokers and included nicotine replacement therapy, electronic cigarettes, heated tobacco, and smokeless tobacco. The OAE reporting was evaluated using an adapted CONSORT Harms checklist. An Adjusted Checklist Score (ACS), representing the proportion of criteria met, was calculated. Univariate linear regressions explored the association between ACS and study-level variables (publication year, country, funding, blinding and product type). Results: OAE reporting was fragmented, with a mean ACS of 0.52 (0.11-0.74). Over 80 % of studies (n=30) provided some quantitative data, but only 53 % (n=19) presented results in a tabulated, arm-specific format. Definitions of OAEs and severity measurement were rarely reported (n=5, 14 % and n=6, 17 % respectively). The method of OAEs collection was described in 50 % of the studies (n=18). OAEs were rarely mentioned in titles (n=4, 11 %) and conclusions (n=13, 36 %). Less than half of the studies reported the reasons for participant withdrawal due to AEs (n=16, 44 %). Only 28 % (n=10) and 44 % (n=16) of the studies reported the analysis approach and statistical methods for AEs, respectively. A weak, non-significant positive correlation was found between ACS and year of publication (r = 0.288, p = 0.09). No study-level variable showed a statistically significant association with ACS. Conclusions: Reporting of OAEs in clinical trials of NCNPs remains limited and inconsistent, often lacking clear definitions, standardized severity assessments, detailed data collection methods, and predefined statistical plans.
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DOI
10.1016/j.jdent.2025.106057
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Preventive Dentistry and Public Oral Health (예방치과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Baek Il(김백일) ORCID logo https://orcid.org/0000-0001-8234-2327
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/207613
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