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Comparison · NCT00772941-e0dbec28

Varenicline - With Antipsychotics as a Concomitant Drug vs Varenicline - Without Antipsychotics as a Concomitant Drug: Risk Factors for the Proportion of Responders - Antipsychotics as a Concomitant Drug.

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Varenicline - With Antipsychotics as a Concomitant Drug vs Varenicline - Without Antipsychotics as a Concomitant Drug: Risk Factors for the Proportion of Responders - Antipsychotics as a Concomitant Drug. Trial comparisons, record NCT00772941-e0dbec28. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00772941-e0dbec28

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.6070.5240.684wilson
Risk in group 20.7810.7650.796wilson
Risk difference, group 1 minus group 2-0.174-0.258-0.0955newcombe hybrid score
Risk ratio, group 1 over group 20.7770.6790.889log
Odds ratio, group 1 over group 20.4330.3050.615log
Number needed to treat, for one fewer participant with the outcome on Varenicline - With Antipsychotics as a Concomitant Drug than on Varenicline - Without Antipsychotics as a Concomitant Drug5.743.8710.5from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Varenicline - With Antipsychotics as a Concomitant DrugVarenicline with Antipsychotics as a Concomitant Drug85140OG000
Group 2Varenicline - Without Antipsychotics as a Concomitant DrugVarenicline without Antipsychotics as a Concomitant Drug2,1112,702OG001

Outcome

Type
PRIMARY
Title
Risk Factors for the Proportion of Responders - Antipsychotics as a Concomitant Drug.
Description
The primary analysis item was the number of participants succeeding with continuous smoking cessation for the previous 4 weeks/the number of participants for efficacy evaluation excluding drop-out participants.
Time frame
24 weeks
Population
The efficacy analysis population basically consists of the evaluable participants in accordance with the separately prepared analysis plan (participants judged to have been evaluated appropriately). The number of participants who provided data on concomitant administration of antipsychotics was 2842.

Source ClinicalTrials.gov

Trial

Title
Drug Use Investigation Of Varenicline (Regulatory Post Marketing Commitment Plan)
NCT number
NCT00772941
Phases
Conditions
Smoking Cessation
Interventions
Varenicline
Lead sponsor
Pfizer
Results first posted
2014-01-24

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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