CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 37 enrolled
Drug / intervention
Varenicline +2 moredrug
Likely dose
Varenicline 1 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00606892
NCT00606892N/ACompleted

Varenicline Attenuates Some of the Subjective and Physiological Effects of Intravenous Nicotine in Humans.

Yale University·interventional·Posted Feb 5, 2008·Updated Sep 25, 2014

In Brief

A clinical study evaluating Varenicline, Placebo, and 1 other intervention for Smoking Cessation. Completed, enrolled 37 participants across 1 site.

Detailed Summary

To examine the effects of varenicline on the subjective, physiological and cognitive responses to intravenous nicotine. Varenicline is a partial nicotine agonist and it is approved as a treatment for smoking cessation. We predict that varenicline treatment will modify subjective, physiological and cognitive responses to IV nicotine.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 5, 2008
Enrollment StartAug 1, 2007
Primary CompletionNov 1, 2008
Study CompletionNov 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 18.4 years ago

Interventions

Vareniclinedrug

Varenicline (1 mg per day) given for 4 days prior to laboratory session

Placebodrug

Sugar Pill

IV Nicdrug

IV Nicotine given during the laboratory session following 4 days of exposure to the study medication (varenicline or placebo). This nicotine was given during each laboratory session which followed the 4 days of exposure to either placebo then varenicline or varenicline then placebo.