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Vaping and Smoking Withdrawal Project

NCT05772845 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 370

Last updated 2026-03-09

No results posted yet for this study

Summary

The proposed research, which will systematically and comprehensively characterize the withdrawal among daily vapers compared to daily smokers of combustible cigarettes, filling critical gaps in the understanding of electronic nicotine delivery systems (ENDS) dependence/abuse liability and contributing to the development of therapies for tobacco/nicotine use, the leading preventable cause of death in the US.

Conditions

  • Acute Abstinence From Cigarettes vs E-cigarettes (ENDS)

Interventions

BEHAVIORAL

Acute (24-hour) abstinence

Participants will be asked to abstain from all tobacco/nicotine for 24 hours prior to the visit

BEHAVIORAL

Ad libitum smoking/vaping

Participants will be asked to smoke/vape as usual during the 24 hours prior to the visit

Sponsors & Collaborators

  • Roswell Park Cancer Institute

    collaborator OTHER

  • National Institute on Drug Abuse (NIDA)

    collaborator NIH

  • State University of New York at Buffalo

    lead OTHER

Principal Investigators

  • Larry Hawk, PhD · University at Buffalo

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-14
Primary Completion
2026-11-30
Completion
2026-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05772845 on ClinicalTrials.gov