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Trial · NCT04377620

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage of Participants Who Have Died Due to Any CauseStudy start to Day 29
To evaluate the 28-day mortality rate of ruxolitinib 5 mg BID + SoC therapy and ruxolitinib 15 mg BID + SoC compared with placebo + SoC therapy, in participants with COVID-19-associated ARDS who require mechanical ventilation.
SecondaryNumber of Ventilator Free DaysStudy start to Day 29Number of days participant did not require mechanical ventilation
SecondaryNumber of ICU Free DaysStudy start to Day 29Number of days participant is out of the ICU
SecondaryOxygen Free DaysStudy start to Day 29Number of days participant did not receive supplemental oxygen
SecondaryVasopressor Free DaysStudy start to Day 29Number of days without use of vasopressor therapy
SecondaryHospital Free DaysStudy start to Day 29Number of days Partcipant is out of the hospital
SecondaryPercentage of Participants With at Least 2-point Improvement in the COVID-19 Ordinal ScaleStudy start to Days 15 and 29Participants with at least 2-point improvement at Day 15 and 29 based on participant state. The scale ranges from 0-8 with 0 being no clinical or virological evidence of infection and 8 being dead
SecondaryPercentage of Participants With at Least 1-point Improvement in the COVID-19 Ordinal ScaleStudy start to Days 15 and 29
Participants with at lest 1-point improvement in clinical status at Days 15 and 29 based on participant state. The scale ranges from 0-8 with 0 being no clinical or virological evidence of infection and 8 being dead
SecondaryTime to Improvement From Baseline Category to Earliest 1-point Improvement in the COVID-19 Ordinal ScaleStudy Start to Day 29TIme to improvement compared to baseline. The scale ranges from 0-8 with 0 being no clinical or virological evidence of infection and 8 being dead
SecondaryPercentage of Participants With the COVID-19 Ordinal Scale ReportedStudy start to Day 29Clinical status of participant at Day 29 based on participant state. The scale ranges from 0-8 with 0 being no clinical or virological evidence of infection and 8 being dead
SecondaryChange in the COVID-19 9-point Ordinal ScaleStudy start to Days 15 and 29Change in the Clinical status of participant at Days 15 and 29 based on participant state. The scale ranges from 0-8 with 0 being no clinical or virological evidence of infection and 8 being dead
SecondaryChange in SOFA Scorefrom baseline to Days 3, 5, 8, 11, 15, and 29
Sequential Organ Failure Assessment (SOFA) score is a scoring system to determine the extent of a person's organ function or rate of failure. The score is based on 6 different scores, 1 each for the respiratory, cardiovascular, hepatic, coagulation, renal, and neurological systems. Each system gets a score from 0 (normal) to 4 (abnormal) and the sum of each score defines the final SOFA score, which 24 is the maximum score (high risk of morality) and 0 is the minimum score (low risk of mortality).
SecondaryNumber and Percentage of Participants With Treatment-related Side Effects and Serious Adverse EventsStudy start to Day 29Treatment-emergent AEs are judged as related by the investigator or have a missing causality.

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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GET https://conductscience.org/api/trials/v1/NCT04377620/registered