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Trial · NCT01594749

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Complete Response From 25 to 120 Hours After Initiation of Moderately Emetogenic Chemotherapy (MEC)Fosaprepitant Regimen78.9Percentage of Participants
Percentage of Participants With Complete Response From 25 to 120 Hours After Initiation of Moderately Emetogenic Chemotherapy (MEC)Control Regimen68.5Percentage of Participants
Percentage of Participants With Infusion-site ThrombophlebitisFosaprepitant Regimen0.6Percentage of Participants
Percentage of Participants With Infusion-site ThrombophlebitisControl Regimen0.0Percentage of Participants
Percentage of Participants With Severe Infusion-site ReactionsFosaprepitant Regimen0.0Percentage of Participants
Percentage of Participants With Severe Infusion-site ReactionsControl Regimen0.0Percentage of Participants
Percentage of Participants With Complete Response From 0 to 120 Hours After Initiation of MECFosaprepitant Regimen77.1Percentage of Participants
Percentage of Participants With Complete Response From 0 to 120 Hours After Initiation of MECControl Regimen66.9Percentage of Participants
Percentage of Participants With Complete Response From 0 to 24 Hours After Initiation of MECFosaprepitant Regimen93.2Percentage of Participants
Percentage of Participants With Complete Response From 0 to 24 Hours After Initiation of MECControl Regimen91.0Percentage of Participants
Percentage of Participants With No Vomiting From 0 to 120 Hours After Initiation of MECFosaprepitant Regimen82.7Percentage of participants
Percentage of Participants With No Vomiting From 0 to 120 Hours After Initiation of MECControl Regimen72.9Percentage of participants

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

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01594749/results