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NCT05239884 · ClinicalTrials.gov registry record · NA

CSD201202: A Study to Assess Nicotine Uptake From Electronic Nicotine Delivery System P12

A NA study of Smoking and Tobacco Use, sponsored by RAI Services Company.

Completed
Registry status
NA
Development phase
36
Enrollment target
1
Study location

NCT05239884 is a NA study of Smoking and Tobacco Use that has completed, run by RAI Services Company. The registered enrollment target is 36 participants, below the 455-participant average among 123 other Smoking trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05239884, a NA study of Smoking and Tobacco Use, has completed, sponsored by RAI Services Company.

COMPLETED
Registry status
NA
Development phase
36 participants
Enrollment target
1
Study location

Study Summary

This is an open-label, randomized, 8-way crossover study designed to evaluate plasma nicotine pharmacokinetic (PK) parameters following an ad libitum use of Electronic Nicotine Delivery System (ENDS) investigational products (IPs) in a confinement setting by generally healthy combustible cigarette (CC) smokers and dual users of CC and ENDS.

Conditions Studied

Interventions

  • OTHER ENDS Product A with 1.5% nicotine
  • OTHER ENDS Product B with 1.5% nicotine
  • OTHER ENDS Product C with 1.5% nicotine
  • OTHER ENDS Product D with 1.5% nicotine
  • OTHER ENDS Product E with 1.5% nicotine

Study Locations (1)

North Carolina

  • High Point Clinical Trials Center - High Point

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2022-03-14
Est. Completion 2022-04-15
Phase NA

Sponsor

RAI Services Company

42 total trials

What the Registry Record Tells You About NCT05239884

The ClinicalTrials.gov registry entry for NCT05239884 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 455-participant average among 123 other Smoking trials with a reported enrollment target (92% lower). The listed sponsor is RAI Services Company, which has 42 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Smoking appearing as the primary indexed condition, and to 5 interventions - of which ENDS Product A with 1.5% nicotine is the first listed.

NCT05239884 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT05239884 about?

NCT05239884 is a clinical study titled "CSD201202: A Study to Assess Nicotine Uptake From Electronic Nicotine Delivery System P12". This is an open-label, randomized, 8-way crossover study designed to evaluate plasma nicotine pharmacokinetic (PK) parameters following an ad libitum use of Electronic Nicotine Delivery System (ENDS) investigational products (IPs) in a confinement setting by generally healthy combustible cigarette (...

What is the current status of trial NCT05239884?

This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2022-03-14. Estimated completion is 2022-04-15.

What conditions does trial NCT05239884 study?

This clinical trial studies the following conditions: Smoking, Tobacco Use.

What interventions are being tested in trial NCT05239884?

The interventions under investigation include: ENDS Product A with 1.5% nicotine (OTHER), ENDS Product B with 1.5% nicotine (OTHER), ENDS Product C with 1.5% nicotine (OTHER), ENDS Product D with 1.5% nicotine (OTHER), ENDS Product E with 1.5% nicotine (OTHER).

Who is sponsoring clinical trial NCT05239884?

This trial is sponsored by RAI Services Company, which has 42 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05239884 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.