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Trial · NCT01023659

Distribution of Bupropion and Varenicline to Increase Smoking Cessation Attempts

NCT01023659, Phase 4, Completed, Centre for Addiction and Mental Health; results first posted 2013-03-15

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Distribution of Bupropion and Varenicline to Increase Smoking Cessation Attempts. Trials, record NCT01023659. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01023659

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Distribution of Bupropion and Varenicline to Increase Smoking Cessation Attempts
NCT number
NCT01023659
Status
Completed
Phases
Phase 4
Enrollment
893 participants, actual
Lead sponsor
Centre for Addiction and Mental Health
Conditions
Tobacco Use Disorder, Smoking, Smoking Cessation
Interventions
bupropion, varenicline, motivational emails
First posted
2009-12-02
Last updated
2018-01-24
Results first posted
2013-03-15

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary7-day Point Prevalence of Abstinence6-month7-day point prevalence of abstinence was assessed by the question "Have you had a cigarette, even a puff, in the past 7 days?"
PrimaryProportion of Eligible Participants Who Were Able to Attend an Appointment With a PhysicianEnd of TreatmentProportion of eligible participants who were able to attend an appointment with a physician to have the prescription signed

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARY7-day Point Prevalence of Abstinence6-month
Number of eligible participants who either received bupropion + motivational emails, varenicline + motivational emails or motivational emails alone (because they either did not attend a physician visit or their physician decided not to prescribe them bupropion or varenicline)
ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYProportion of Eligible Participants Who Were Able to Attend an Appointment With a PhysicianEnd of Treatmenttotal number of eligible participants in studyParticipantsCOUNT_OF_PARTICIPANTS

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
7-day Point Prevalence of AbstinenceBupropion + Motivational Emails45Participants
7-day Point Prevalence of AbstinenceMotivational Emails22Participants
7-day Point Prevalence of AbstinenceVarenicline + Motivational Emails50Participants
Proportion of Eligible Participants Who Were Able to Attend an Appointment With a PhysicianAll Eligible Participants588Participants

Participant flow9

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDBupropion + Motivational Emails258
Overall StudySTARTEDMotivational Emails365
Overall StudySTARTEDVarenicline + Motivational Emails264
Overall StudyCOMPLETEDBupropion + Motivational Emails185
Overall StudyCOMPLETEDMotivational Emails137
Overall StudyCOMPLETEDVarenicline + Motivational Emails165
Overall StudyNOT COMPLETEDBupropion + Motivational Emails73
Overall StudyNOT COMPLETEDMotivational Emails228
Overall StudyNOT COMPLETEDVarenicline + Motivational Emails99

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityBupropion + Motivational Emails
Total, all-cause mortalityMotivational Emails
Total, all-cause mortalityVarenicline + Motivational Emails
Total, other adverse eventsBupropion + Motivational Emails00
Total, other adverse eventsMotivational Emails00
Total, other adverse eventsVarenicline + Motivational Emails00
Total, serious adverse eventsBupropion + Motivational Emails00
Total, serious adverse eventsMotivational Emails00
Total, serious adverse eventsVarenicline + Motivational Emails00

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
26429100RESULT

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01023659

GET https://conductscience.org/api/trials/v1/NCT01023659/registered