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Comparison · NCT00772941-dc104cc2

Administration Prolonged After 12 Weeks vs Administration Not Prolonged After 12 Weeks: Risk Factors for the Proportion of Responders - Prolonged Administration After 12 Weeks.

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. Administration Prolonged After 12 Weeks vs Administration Not Prolonged After 12 Weeks: Risk Factors for the Proportion of Responders - Prolonged Administration After 12 Weeks. Trial comparisons, record NCT00772941-dc104cc2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00772941-dc104cc2

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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 10.6090.4870.719wilson
Risk in group 20.7870.770.802wilson
Risk difference, group 1 minus group 2-0.177-0.301-0.0658newcombe hybrid score
Risk ratio, group 1 over group 20.7750.6360.944log
Odds ratio, group 1 over group 20.4230.2540.706log
Number needed to treat, for one fewer participant with the outcome on Administration Prolonged After 12 Weeks than on Administration Not Prolonged After 12 Weeks5.653.3315.2from 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 1Administration Prolonged After 12 WeeksParticipants with prolonged administration of Varenicline after 12 weeks according to Japanese Package Insert.3964OG000
Group 2Administration Not Prolonged After 12 WeeksParticipants without prolonged administration of Varenicline after 12 weeks according to Japanese Package Insert.1,9932,534OG001

Outcome

Type
PRIMARY
Title
Risk Factors for the Proportion of Responders - Prolonged Administration After 12 Weeks.
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 in whom the prolonged administration of Varenicline after 12 weeks was confirmed was 2598.

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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