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A
Smoking Cessation Trial with Lobeline Sulfate: A Pilot Study
Elbert
D. Glover, PhD; Scott J. Leischow, PhD; Stephen I. Rennard, MD;
Penny N. Glover, MEd, CCRC; David Daughton, MS; John N. Quiring,
PhD; F. Howard Schneider, PhD; Peter J. Mione, MS
Objective:
To evaluate a sublingual formulation of lobeline sulfate for smoking
cessation. Methods: Random assignment of 180 healthy smokers
to treatment (n=90) or placebo (n=90). Treatment was self-administering
a 7.5 mg lobeline sulfate sublingual or placebo tablet 9 times per
day for 6 weeks. Results: No difference in cessation efficacy
between placebo and active treatment. Among highly dependent smokers
who completed the trial, there was a trend for higher cessation
rates in the active group. Conclusion: This pilot study failed
to demonstrate smoking-cessation efficacy. However, data suggest
continued studies to evaluate lobeline sulfate for smoking cessation.
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