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Trial · NCT01156792

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTrough (AM Pre-dose and Pre-rescue Bronchodilator) Forced Expiratory Volume in 1 Second (FEV1) at the End of the 6-week Treatment PeriodEnd of Week 6ITT Population. Only those participants available at the specified time point were analyzed.Liters (L)LEAST_SQUARES_MEAN
SECONDARYDaily Trough (Morning Pre-dose and Pre-rescue Bronchodilator) Morning Peak Expiratory Flow (PEF) Averaged Over the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Liters/minute (L/min)LEAST_SQUARES_MEAN
SECONDARYDaily Evening PEF Averaged Over the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.L/minLEAST_SQUARES_MEAN
SECONDARYDaily (Average of Morning and Evening) PEF Averaged Over the Last 3 Weeks of the 6 -Week Treatment Period Between GSK2190915 and Montelukast GroupsWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.L/minLEAST_SQUARES_MEAN
SECONDARYDaily Asthma Symptom Score Averaged Over the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Score on a scaleLEAST_SQUARES_MEAN
SECONDARYDaily Rescue Short-acting beta2-agonist (SABA) Use Averaged Over the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Number of inhalationsLEAST_SQUARES_MEAN
SECONDARYPercentage of Symptom-free Days During the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Percentage of daysLEAST_SQUARES_MEAN
SECONDARYPercentage of Symptom-free Nights During the Last 3 Weeks of the 6 Week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Percentage of nightsLEAST_SQUARES_MEAN
SECONDARYPercentage of Rescue-free Days During the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Percentage of daysLEAST_SQUARES_MEAN
SECONDARYPercentage of Rescue-free Nights During the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Percentage of nightsLEAST_SQUARES_MEAN
SECONDARYPercentage of Nights Without Awakenings Due to Asthma During the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population. Only those participants available at the specified time point were analyzed.Percentage of nightsLEAST_SQUARES_MEAN
SECONDARYNumber of Participants Withdrawn Due to Lack of Efficacy During the Last 3 Weeks of the 6-week Treatment PeriodWeek 4 to Week 6ITT Population.Number of participantsNUMBER

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01156792/outcomes