Actively Recruiting

Early Phase 1
Age: 21Years - 55Years
All Genders
Healthy Volunteers
NCT06066996

Evaluation of the Electronic Cigarette Withdrawal Syndrome

Led by Johns Hopkins University · Updated on 2025-07-14

150

Participants Needed

1

Research Sites

239 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this project is to rigorously evaluate the nature of e-cigarette withdrawal in exclusive e-cigarette users during a monitored abstinence period and the role of nicotine in the expression of this withdrawal syndrome.

CONDITIONS

Official Title

Evaluation of the Electronic Cigarette Withdrawal Syndrome

Who Can Participate

Age: 21Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 21 to 55 years old
  • Good general health as reviewed by the study medical team
  • Vital signs within normal range as reviewed by the study medical team
  • Negative urine test for illicit drugs (excluding THC) and negative breath alcohol test
  • Daily use of a nicotine-containing e-cigarette for at least 6 months
  • No regular use of other tobacco products for at least 6 months
  • Urine cotinine greater than 100 ng/mL to confirm current nicotine use
  • Exhaled breath carbon monoxide less than 6 ppm
  • Penn State E-cigarette Dependence score of 4 or higher indicating mild dependence or greater
  • Interest in reducing e-cigarette use
Not Eligible

You will not qualify if you...

  • Psychoactive drug use (other than cannabis, nicotine, alcohol, caffeine) in the past month
  • Current use of over-the-counter or prescription medications that may impact safety
  • Use of cannabis more than twice per week
  • History or current significant medical condition impacting participation or safety
  • Current psychiatric condition or substance use disorder (except tobacco use disorder) impacting participation or safety
  • Enrollment in another clinical trial
  • Positive pregnancy test
  • Currently using nicotine or tobacco cessation products
  • Seizure disorder or traumatic brain injury

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Behavioral Pharmacology Research Unit

Baltimore, Maryland, United States, 21224

Actively Recruiting

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Research Team

J

Justin Strickland, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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