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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04525755
Other study ID # Pro00098479
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date February 8, 2021
Est. completion date September 2025

Study information

Verified date March 2024
Source Medical University of South Carolina
Contact Amy Boatright
Phone 843-876-2440
Email boatrigh@musc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a research study to find out if a smoking cessation medications, either varenicline or nicotine replacement products (patches or lozenges), are effective when given to smokers, remotely, as a one-time sample. Participants will either receive a sample of varenicline, nicotine patches and lozenges, or neither. This will be decided randomly. Participants have a 50%chance of receiving varenicline, a 25% chance of receiving nicotine products, and a 25% chance of receiving neither. If the participant is assigned to a group that receives free samples, they will be mailed to them free of charge. There is no requirement to use them, and it is completely up to the participants. There is also no requirement to quit in this study. The study lasts for six months, and will involve six total surveys. In addition, investigators ask that participants complete daily diaries (about 1 minute each) for the first 4 weeks of the study. Both varenicline and nicotine replacement products are well-established medications that help smokers quit.


Recruitment information / eligibility

Status Recruiting
Enrollment 648
Est. completion date September 2025
Est. primary completion date March 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Eligibility criteria include: 1. age 18+; 2. daily smoker (25+ days per previous month); 3. smoking 5+ cigarettes/day; 4. smoking > 1yr; 5. some interest in eventual quitting (>2 on 10-point scale); 6. has a primary care doctor and has seen that doctor at least once in past year; 7. not currently pregnant, breastfeeding, or planning to become pregnant; 8. no suicidal ideation in past month, nor any lifetime suicide attempt; 9. no reports of hallucinations; 10. no reports of history of seizures; nor cardiac/renal disease 11. own a smartphone or have regular (daily) access/use of email 12. if female, willing to take a pregnancy test 13. not currently taking any medications to help quit smoking 14. no diagnosis of schizophrenia or bipolar disorder 15. no members of the same household currently enrolled in the study

Study Design


Intervention

Drug:
Varenicline 0.5 MG
varenicline comes in bottles of 56 - 0.5 mg pills
Nicotine Replacement Therapy (NRT)
28 day supply of nicotine patch (1 patch x 28 days @ 14 mg) and lozenge (14 per day x 28 days @ 4 mg)

Locations

Country Name City State
United States Medical University of South Carolina Charleston South Carolina

Sponsors (1)

Lead Sponsor Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 7-day Quit Attempts Percentage of participants With 7-day self-reported point prevalence abstinence, among smokers randomized to a) varenicline, b) NRT, or c) no sampling control group From study enrollment through end of six-month follow up
Secondary Reduction in Smoking Percentage of participants who have reduces their smoking by at least 50%, at both Week 4 and Week 26 follow-up, among smokers randomized to a) varenicline, b) NRT, or c) no sampling control group At the week 4 follow up and week 26 follow up.
Secondary Any Quit Attempts Any self-defined attempt to stop smoking cigarettes among smokers randomized to a) varenicline, b) NRT, or c) no sampling control group From study enrollment through end of six-month follow up
Secondary Use of Smoking Cessation Medication Use of any smoking cessation medication among smokers randomized to a) varenicline, b) NRT, or c) no sampling control group From study enrollment through end of six-month follow up
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