Trial · NCT04291508
Outcomes21
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 21
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Days Alive and Free of Organ Support to Day 28 | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| PRIMARY | 28-day All Cause Mortality | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Days Free of Assisted Ventilation to Day 28 | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| PRIMARY | Days Free of Renal Replacement Therapy to Day 28 in Overall Cohort | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| PRIMARY | Days Free of Vasopressors to Day 28 in Overall Cohort | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | Ventilator-free Days (VFD) | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | Vasopressor-free Days | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | Renal Replacement-free Days | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | 28 Day Hospital Mortality | 28 days after randomization | Data needed to determine this outcome was missing in 3 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | ICU Free Days | 28 days after randomization | Data needed to determine this outcome was missing in 4 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | Hospital Free Days to Discharge Home | Up to day 28 | Data needed to determine this outcome was missing in 3 patients in the Acetaminophen active arm and 2 patients in the Acetaminophen placebo arm. | days | MEAN |
| SECONDARY | Number of Subjects With Initiation of Assisted Ventilation | Up to day 28 | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Subjects With Initiation of Renal Replacement Therapy | Up to day 28 | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Change in Organ-specific Sepsis-related Organ Failure Assessment (SOFA) Scores Between Enrollment and Study Day 7 | Day 0-Day 7 | score on a scale | MEAN | |
| SECONDARY | Renal Calculi to Day 90 | Up to day 90 | Renal calculi diagnosed between randomization and study day 90 in patients in the Vitamin C-Active/Vitamin C-Placebo group. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 90-day All-cause Mortality | 90 days after randomization | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | 90-day Hospital Mortality | 90 days after randomization | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Subjects Who Developed ARDS Within 7 Days of Randomization | Up to day 7 | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Change in Serum Creatinine Concentration | Up to day 28 | mg/dL | MEAN | |
| SECONDARY | Number of Subjects With Major Adverse Kidney Events at 28 Days (MAKE28) | 28 days after randomization | Participants | COUNT_OF_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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT04291508/outcomes