Trial · NCT06042855
Outcomes17
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 17 of 17
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Time to Sustained Recovery in Days | Up to 28 days | Participants with sustained recovery. | days | MEDIAN |
| PRIMARY | Number of Participants With Hospitalization or Death | Up to 28 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants With Mortality | Up to 28 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Time to Mortality | Up to 28 days | Data not collected due to no participants having mortality. | ||
| SECONDARY | Number of Participants With Hospitalization, Urgent Care, Emergency Room Visit, or Death | Up to 28 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants at Each Score on the COVID Clinical Progression Scale at Day 7 | Day 7 | Participants with COVID clinical progression scale data available. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants at Each Score on the COVID Clinical Progression Scale at Day 14 | Day 14 | Participants who had COVID clinical progression scale data available. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants at Each Score on the COVID Clinical Progression Scale at Day 28 | Day 28 | Participants who had COVID clinical progression scale data available. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Physical Function | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Fatigue | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Pain | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Depression | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Anxiety | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Social | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Quality of Life (QOL) as Measured by the PROMIS-29 - Sleep | Day 7, 14, 28, 90, 120, and 180 | Participants with data collected at each timepoint. | score on a scale | MEDIAN |
| SECONDARY | Time Unwell in Days as Measured by the Symptom and Clinical Event Scale | Up to 14 days | Participants with time unwell. | days | MEAN |
| SECONDARY | Mean Days Benefit as Measured by the Symptom and Clinical Event Scale | Up to 14 days | Participants with time unwell. | days | MEAN |
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/NCT06042855/outcomes