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Trial · NCT00772941

Results by group26

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

OutcomeGroupCategoryValueSpreadUnits
Risk Factors for the Frequency of Treatment Related Adverse Events - Gender.Male377participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Gender.Female336participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Age.<65 Years571participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Age.>=65 Years142participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Chronic Obstructive Pulmonary Disease as a Complication.Varenicline - With Chronic Obstructive Pulmonary Disease23participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Chronic Obstructive Pulmonary Disease as a Complication.Varenicline - Without Chronic Obstructive Pulmonary Disease690participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Concomitant Drugs.Varenicline - With Concomitant Drugs289participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Concomitant Drugs.Varenicline - Without Concomitant Drugs424participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Concomitant Therapies.Varenicline - With Concomitant Therapies45participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Concomitant Therapies.Varenicline - Without Concomitant Therapies668participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.<40 kg at Baseline6participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.>=40 kg and <50 kg at Baseline98participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.>=50 kg and <60 kg at Baseline135participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.>=60 kg and <70 kg at Baseline110participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.>=70 kg and <80 kg at Baseline61participants
Risk Factors for the Frequency of Treatment Related Adverse Events - Weight at Baseline.>= 80 kg at Baseline31participants
Risk Factors for the Proportion of Responders - Tobacco Consumption Per Day.<=20 Cigarettes Per Day1299participants
Risk Factors for the Proportion of Responders - Tobacco Consumption Per Day.>=21 and <=40 Cigarettes Per Day817participants
Risk Factors for the Proportion of Responders - Tobacco Consumption Per Day.>=41 Cigarettes Per Day66participants
Risk Factors for the Proportion of Responders - Prolonged Administration After 12 Weeks.Administration Prolonged After 12 Weeks39participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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