Cigarette Packaging of Low Nicotine Cigarettes

  • STATUS
    Recruiting
Updated on 19 February 2024

Summary

The purpose of this study is to examine the effects of smoking non-menthol, investigational low nicotine cigarettes in different types of packaging.

Description

During 8 in-person sessions at our Center, you will provide us with breath samples, answer questionnaires, and smoke two cigarettes in our Center’s well-ventilated smoking rooms. After the second session, our Center will provide you with study cigarettes that you will smoke for the remainder of the study at no cost. At two of the sessions, you will also be asked to provide a small urine sample. Over the course of the entire study, we will ask you to collect your used cigarette filters in bags provided by the Center. You will be asked to bring these filter collection bags with you to each session.
 
The entire study will take approximately 5 weeks for you to complete. You will be asked to attend 8 in-person sessions every 4-6 days. Most sessions will be about 2 hours long. This is not a quit smoking study. Participants will be compensated for their time and effort for each session they complete.

FAQ


For more information and to see if you are eligible, please call 215-746-5786.

Details
Condition smoking,nicotine,behavior
Age 21years - 65years
Clinical Study IdentifierNCT03802019
Last Modified on19 February 2024

Eligibility

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team


Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact
Race
Ethnicity
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.