Trial · NCT06729606
Results by group20
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 20
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 1 = at home and off oxygen (recovered) for at least 77 days | 36 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 1 = at home and off oxygen (recovered) for at least 77 days | 31 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 2 = at home and off oxygen for 49-76 days | 37 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 2 = at home and off oxygen for 49-76 days | 35 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 3 = at home and off oxygen for 1-48 days | 43 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 3 = at home and off oxygen for 1-48 days | 32 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 4 = not hospitalized but either on supplemental oxygen or not at home | 15 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 4 = not hospitalized but either on supplemental oxygen or not at home | 31 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 5 = hospitalized or in hospice care | 8 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 5 = hospitalized or in hospice care | 13 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Aviptadil + SOC | category 6 = died | 86 | Participants | |
| Number of Participants With a 6-category Primary Ordinal Outcome (Recovery) at Day 90 | Placebo + SOC | category 6 = died | 83 | Participants | |
| Number of Participants Who Died Through Day 90 | Aviptadil + SOC | 86 | Participants | ||
| Number of Participants Who Died Through Day 90 | Placebo + SOC | 83 | Participants | ||
| Number of Participants With a Safety Outcome Through Day 5 | Aviptadil + SOC | 146 | Participants | ||
| Number of Participants With a Safety Outcome Through Day 5 | Placebo + SOC | 129 | Participants | ||
| Number of Participants With a Safety Outcome Through Day 28 | Aviptadil + SOC | 181 | Participants | ||
| Number of Participants With a Safety Outcome Through Day 28 | Placebo + SOC | 172 | Participants | ||
| Number of Participants Who Died Through Day 180 | Aviptadil + SOC | 90 | Participants | ||
| Number of Participants Who Died Through Day 180 | Placebo + SOC | 86 | 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
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT06729606/results