Ready to quit smoking?

This is an opportunity at a new treatment that could help you finally quit smoking for good. The CAST Study has limited space. Sign up now.

We're looking for volunteers who are...
- Between the age of 21-65

- Ready to switch from cigarettes to e-cigarettes

- Willing to take study medication

- Currently smoke 10 or more cigarettes per day, but want to stop

- Able to pass a urine drug test

- Not experiencing any serious medical conditions

- Not using other tobacco products in the last 14 days (including cigars, pipes, hookahs, e-cigarettes, or nicotine replacement therapy.)

Sign-up to participate

Volunteer information will be reviewed by our team and you will be contacted for this study and your interest in future studies.

Participant Short Web To Lead

By clicking submit you agree to the Rose Research Center Terms and Conditions and that we may contact you via text, email, and/or phone unless you later withdraw your consent. Message and data rates may apply.


What are the benefits to participating in this Clinical Trial?
Gain access to new research treatments before they are widely available and potentially Quit Smoking
What are the risks to participating in a Clinical Trial?
Side effects will differ from study to study, you will be informed of any expected side effects when you come in for your first visit as well as in the consent form.
How long with the Clinical Trial last?
This trial lasts 10 weeks and we will require you come into our office 6 times.
Will I receive compensation for my participation?
Yes. If you come to all your visits and complete all your questionnaires you will earn as much as $1,175.

Additionally, we hope you may have quit smoking.
Do I need to ask my regular doctor before I can participate in a research study?
Not unless you want to.
You may want to share with them that you will be taking centanafadine to potentially help you quit smoking. Your doctor may wish to contact our study doctor (with your permission) to request additional information.
What is informed consent?
The informed consent process provides you with the information required to ensure you make an informed decision about participation in the clinical research study. This process will:

  • Help you to understand the information
  • Give you an opportunity to ask questions and to consider whether to participate
  • Obtain your voluntary agreement to participate
  • Continue to provide information as the clinical research study progresses

Before participating, we will take you through a written Informed Consent Form (ICF) that outlines the important information to consider before joining the study. The study doctor will go through this document with you and answer any questions you may have. This document provides details of the study, such as study expectations, duration, and what you will need to do. All known possible risks and potential benefits are also explained in the ICF.

After you have read and discussed all of the information about the study, you can decide whether or not to sign the consent form. This consent form is not a contract and you are always free to leave the study at any time and for any reason, with no penalty to you. Additionally, during your participation, the study doctor will let you know in a timely manner of any information that may change your mind about participating.
Why should I participate?
To help you quit smoking. According to the CDC, smoking is still the number one leading cause of preventable death in the United States.

Ready to quit? Sign-up today!

Fill out our form below for more information. Participant information is maintained in a volunteer database system and retained for this study and future studies as they become available. You can opt-out at any time. Pertinent information is confidentially kept on file to aid in selecting highly qualified candidates for research studies.

Quit Smoking Studies Lead Form

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