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N/A N=56 Randomized Triple-blind Other

Novel Medication as a Potential Smoking Cessation Aid

Tobacco Use Disorder

Enrolled (actual)
56
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcome: Primary: Percent of Days of Confirmed Abstinence (Out of 5 Maximum) — 46.9; 42.0 percentage of days non-smoking

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Levomilnacipran (Drug); Placebo (Drug)
Age
Adult · 25+ yrs
Sex
All
Sponsor
University of Minnesota
Primary completion
May 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent of Days of Confirmed Abstinence (Out of 5 Maximum)
46.9; 42.0

Summary

The purpose of this study is to provide preliminary information assessing if levomilnacipran may be effective at increasing smoking cessation rates.

Eligibility Criteria

Inclusion Criteria

  • Be between 25 years old and 55 years old
  • Smoke a minimum number of cigarettes per day
  • Indicate motivation to quit smoking

Exclusion Criteria

  • Current or history of medical or psychiatric conditions that could interfere with measures being studied or that could be affected by the study medication
  • Use of medication that could interfere with measures to be studied or that could be expected to interact with levomilnacipran
  • Are pregnant or breast feeding

The investigators will evaluate if there are other reasons why someone may not be eligible to participate

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02265367). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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