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NCT05280769

Effects of an Oral Nicotine Product in Smokeless Tobacco Users

Completed NA Last updated 2 October 2024
What this trial tests

NA trial testing oral nicotine pouch - 2 mg in Tobacco Use in 31 participants. Completed in 28 November 2023.

Timeline
23 August 2022
Primary endpoint
28 November 2023
28 November 2023

Quick facts

Lead sponsorVirginia Commonwealth University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment31
Start date23 August 2022
Primary completion28 November 2023
Estimated completion28 November 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Virginia Commonwealth University

Who can join

Adults 18 to 55, any sex, with Tobacco Use. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research study is to find out how three different nicotine pouches and participant's own brand of smokeless tobacco affect blood nicotine levels and how participants feel.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Physiological and subjective effects of an oral nicotine pouch in people who use smokeless tobacco.
    Eversole A, Imran R, Gaitan N, Cobb CO, et al · · 2025 · PMID 40839513 · DOI 10.1037/pha0000798

Verify or expand the search:

Other recruiting trials for Tobacco Use

Currently open trials in the same condition.

Other Virginia Commonwealth University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05280769.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing