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Trial · NCT04579393

Outcomes20

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With at Least 1 Serious Adverse EventDay 29Intention-to-treat analysisParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants With Sustained Recoveries Defined by Ordinal Scale Score of 3 or Lessday 29ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants Who Progress to Mechanical Ventilationday 29Participants who were not receiving mechanical ventilation at baselineParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants With Cumulative Clinical Endpoint of Deathday 14, day 28, day 60Intention-to-treat analysisParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Grade 3 and 4 Adverse Events Through Day 60Day 60Intention-to-treat analysisAdverse EventsNUMBER
SECONDARYParticipant Score on Ordinal ScaleDay 15, Day 29intent to treat analysisscore on a scaleMEDIAN
SECONDARYChange in C-Reactive Protein Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
mg/L (milligrams per liter)MEDIAN
SECONDARYChange in Fibrinogen Levels From Baseline.Day 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
mg/dL (milligrams per decilitre)MEDIAN
SECONDARYChange in D-Dimer Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
mcg/mL (microgram per milliliter)MEDIAN
SECONDARYChange in Ferritin Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
mcg/L (micrograms per liter)MEDIAN
SECONDARYChange in Interleukin 6 (IL6) Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
pg/mL (picograms per milliliter)MEDIAN
SECONDARYMedian Days Participants Were Admitted to Intensive Care UnitDay 29Participants admitted to Intensive Care UnitDaysMEDIAN
SECONDARYRelative Change in SpO2/FiO2 RatioDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Only SpO2/FiO2 ratio is available as PaO2 was not consistently measured. Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
SpO2/FiO2 ratioMEDIAN
SECONDARYChange in SOFA Score From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
score on a SOFA scaleMEDIAN
SECONDARYMedian Days on Participants Received Supplemental Oxygenday 29daysMEDIAN
SECONDARYThe Number of Participants That Experienced Acute Renal Failureday 29Intent to treat analysisParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants That Experienced a Deep Vein Thrombosis (DVT) or Pulmonary Embolism (PE)day 29Intent to Treat Analysis.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYChange in Absolute Lymphocyte Count Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
thousand cells per microliterMEDIAN
SECONDARYChange in Absolute Neutrophil Count Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
thousand cells per microliterMEDIAN
SECONDARYChange in Platelet Count Levels From BaselineDay 3, Day 5, Day 8, Day 11, Day 15, Day 29
Intent to treat analysis. 58 patients (29 in each group) provided research samples for at least one time-point since baseline except for one patient who did not take any study drug and withdrew consent after enrollment.
thousand cells per microliterMEDIAN

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/NCT04579393/outcomes