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Trial · NCT05770466

Registered outcomes13

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

ListOutcomeTime frameDescription
PrimaryProportion of patients who are negative to SARS-CoV-2 at Day 8Up to Day 8Proportion of patients who are negative to SARS-CoV-2 based on quantitative (Ct value ≥30) RT-PCR at Day 8 or discharge before Day 8 due to recovery
PrimaryTime to discharge from hospitalUp to Day 29Time to discharge from hospital according to the latest Taiwan CDC guidance for SARS-CoV-2 infection (From randomization to discharge)
SecondaryProportion of patients who are negative to SARS-CoV-2 at Day 5Up to Day 5Proportion of patients who are negative to SARS-CoV-2 based on quantitative (Ct value ≥30) RT-PCR at Day 5 or discharge before Day 5 due to recovery
SecondaryChange in clinical status of patient at Day 5Up to Day 5Change in clinical status of patient on WHO clinical progression scale at Day 5
SecondaryChange in clinical status of patient at Day 8Up to Day 8Change in clinical status of patient on WHO clinical progression scale at Day 8
SecondaryChange of SpO2Up to Day 29Change of SpO2 from baseline
SecondaryTime from symptom onset to resolution of clinical signs and symptomsUp to Day 29Time from the onset of clinical symptoms related to COVID-19 (e.g., fever, cough, dyspnea or change in taste or smell) to the resolution of clinical signs and symptoms.
SecondaryTime from symptom onset to RT-PCR negative resultUp to Day 29Time from the onset of clinical symptoms related to COVID-19 (e.g., fever, cough, dyspnea or change in taste or smell) to the RT-PCR negative result (Ct value ≥30).
SecondaryTime from RT-PCR positive result to the resolution of clinical signs and symptomsUp to Day 29Time from RT-PCR positive result (Ct value \< 30) to the resolution of clinical signs and symptoms related to COVID-19 (e.g., fever, cough, dyspnea or change in taste or smell)
SecondaryTime from RT-PCR positive result to RT-PCR negative resultUp to Day 29Time from RT-PCR positive result (Ct value \< 30) to RT-PCR negative result (Ct value ≥30)
SecondaryOccurrence and duration (days) of supplemental oxygenUp to Day 29Occurrence and duration (days) of supplemental oxygen
SecondaryOccurrence and duration (days) of mechanical ventilationUp to Day 29Occurrence and duration (days) of mechanical ventilation
SecondaryTime to treatment with other antiviral agents within 8 daysUp to Day 8To evaluate the time to treatment with other antiviral agents within 8 days in the Ropeginterferon alfa-2b treatment group,

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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