Mechanistic Evaluations of Pre-Cessation Therapies for Smoking Cessation

NCT01406223 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 282

Last updated 2017-11-14

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to look at brain function in order to understand how different treatments work to help people quit smoking. In this study, the investigators will look at the effects of nicotine patches, Chantix alone or Chantix paired with Zyban.

Conditions

  • Nicotine Dependence

Interventions

DRUG

Varenicline

DRUG

Bupropion

DRUG

Nicotine patches

OTHER

Placebo varenicline

OTHER

Placebo bupropion

OTHER

Placebo patch

Sponsors & Collaborators

  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • Duke University

    lead OTHER

Principal Investigators

  • F. Joseph McClernon, Ph.D. · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2013-12-31
Completion
2014-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01406223 on ClinicalTrials.gov