Baltimore, MDNCT07128329Now EnrollingIRB Ready

Nicotine Pouch Self-Administration Clinical Trial in Baltimore, MD

Access cutting-edge nicotine pouch self-administration treatment through this clinical trial at a research site in Baltimore. Study-provided care at no cost to qualified participants.

Sponsored by Johns Hopkins University

Quick Self-Assessment

See if you qualify for this Baltimore location

Preparing your pre-screening questions…

Expert Care in Baltimore

Access nicotine pouch self-administration specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related nicotine pouch self-administration treatment provided free

Apply for This Baltimore Location

Check if you qualify for this nicotine pouch self-administration clinical trial in Baltimore, MD

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Baltimore

    Convenient for MD residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Baltimore site if eligible
  4. 4Begin participation

About This Nicotine Pouch Self-Administration Study in Baltimore

The present human laboratory study will recruit cigarette smokers (n=60) and adult infrequent nicotine users (n=60) to complete two counterbalanced lab sessions in which the participants use nicotine pouches under controlled conditions. The investigators are recruiting both frequent and infrequent nicotine users because FDA regulates tobacco products based on a public health standard, meaning FDA must consider the impact a regulation may have on the population as a whole (e.g., people who use and do not use tobacco products currently).

Sponsor: Johns Hopkins University

Who Can Participate

Inclusion Criteria

(all participants):
greater than or equal to 21 years old
good general health based on screening procedures
vital signs in normal range (resting heart rate less than 110bpm, systolic blood pressure less than 150mmHg, diastolic blood pressure less than 100mmHg)
negative urine test for illicit drug use (excluding THC) and negative breath alcohol test at screening and before each session
no self-reported prior use of oral nicotine pouches
Not actively trying to quit smoking or using smoking cessation medication (e.g., nicotine replacement therapy) Additional inclusion criteria (smokers):
self-report currently smoking cigarettes daily
exhaled breath CO greater than or equal to 10ppm and urine cotinine greater than 100 ng/ml at screening
meet criteria for tobacco use disorder
no self-reported regular use of other tobacco products (e.g., smokeless products, e-cigarettes) in the past 30 days Additional inclusion criteria (non-nicotine users):
self-report previously using nicotine/tobacco but no more than 100 lifetime uses across all routes of administration
no self-reported nicotine/tobacco uses in the past 30 days
urine cotinine less than 100 ng/ml at screening.

Exclusion Criteria

(all participants):
psychoactive drug use (aside from cannabis, nicotine, alcohol, or caffeine) in past month
current use of OTC drugs, supplements/vitamins, or prescription medications that, in the opinion of medical staff, will impact safety
currently have severe dependence for cannabis
history of or current significant medical condition that, in the opinion of medical staff, will impact safety
current psychiatric condition or substance use disorder (aside from tobacco use disorder for smokers), that, in the opinion of medical staff, will impact safety
women who are pregnant, planning to become pregnant, or are breast-feeding

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Baltimore?

Yes, this clinical trial (NCT07128329) has an active research site in Baltimore, MD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Nicotine Pouch Self-Administration Treatment Options in Baltimore, MD

If you're searching for nicotine pouch self-administration treatment options in Baltimore, MD, this clinical trial (NCT07128329) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Baltimore research site is actively enrolling participants for this clinical trial. You'll receive care from experienced nicotine pouch self-administration specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all nicotine pouch self-administration clinical trials near you to find additional studies recruiting in your area.

Ready to Join in Baltimore?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Baltimore, MD