Trial · NCT00978419
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Primary Endpoint: Reduction in CRP Level Over Time, Compared to Placebo Measured at Baseline and Days 3, 7, 14. The Mean CRP Levels at Specified Days Will be the Endpoints. | Days 1, 3, 7, 14 | |
| Secondary | Mortality Compared to Placebo | 90 days | |
| Secondary | Mortality Compared to Placebo, Adjusted for Cardiovascular Co-morbidities | 90 days | |
| Secondary | Reduction in the Incidence of Septic Shock (See Definition) Compared to Placebo | 28 days | |
| Secondary | Reduction in the Incidence of Septic Shock (See Definition) Compared to Placebo, Adjusted for Cardiovascular Co-morbidities | 28 days | |
| Secondary | A Reduction in CK Levels Over Time, Compared to Placebo Measured at Baseline and Days 3, 7, 14, 21, 28 | 28 days | |
| Secondary | A Reduction in ALT Levels Over Time, Compared to Placebo, Measured at Baseline, Days 1, 7, 14, 21, 28 | 28 days | |
| Secondary | Determine the Safety of Rosuvastatin Compared to Placebo in Burn Patients by Comparing the Frequency, Type and Severity of Adverse Events | 28 days | |
| Secondary | Determine Which Are Appropriate Attainable Endpoints for Future Trials and the Number of Participants Required to Reach Significance in Analysis of a Variety of Variables | 28 days | |
| Secondary | Determine the Prevalence of Delirium in the Two Subgroup of Patients | 28 days | |
| Secondary | Determine the Prevalence of De-novo Long-term Neurocognitive Impairment in Burn Patients and by Study Group. | 90 days | |
| Secondary | Determine the Prevalence of Functional Impairment in Burn Patients and by Study Group | 90 days |
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/NCT00978419/registered