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Trial · NCT01475721

Results by group14

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Experiencing an Event in the Composite Safety Endpoint of Serious Asthma Outcomes ( Asthma-related Hospitalization, Asthma-related Endotracheal Intubation, or Asthma-related Death)
Fluticasone Propionate/Salmeterol Combination (FSC)34Participants
Number of Participants Experiencing an Event in the Composite Safety Endpoint of Serious Asthma Outcomes ( Asthma-related Hospitalization, Asthma-related Endotracheal Intubation, or Asthma-related Death)
Fluticasone Propionate (FP)33Participants
Number of Participants Experiencing at Least One Asthma ExacerbationFluticasone Propionate/Salmeterol Combination (FSC)480Participants
Number of Participants Experiencing at Least One Asthma ExacerbationFluticasone Propionate (FP)597Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate/Salmeterol Combination (FSC)Hospitalization34Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate (FP)Hospitalization33Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate/Salmeterol Combination (FSC)Endotracheal intubation0Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate (FP)Endotracheal intubation2Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate/Salmeterol Combination (FSC)Death0Participants
Number of Participants Experiencing at Least One Asthma Related Hospitalization , Endotracheal Intubation and DeathFluticasone Propionate (FP)Death0Participants
Number of Participant Withdrawals From Study Treatment Due to Asthma ExacerbationFluticasone Propionate/Salmeterol Combination (FSC)66Participants
Number of Participant Withdrawals From Study Treatment Due to Asthma ExacerbationFluticasone Propionate (FP)84Participants
Mean Rescue Medication (Albuterol/Salbutamol) Use as Puffs Per 24 HoursFluticasone Propionate/Salmeterol Combination (FSC)0.90Standard Error 0.018Number of Puffs
Mean Rescue Medication (Albuterol/Salbutamol) Use as Puffs Per 24 HoursFluticasone Propionate (FP)1.09Standard Error 0.020Number of Puffs

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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