Name (Synonyms) | Correlation | |
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drug254 | ArtemiC Wiki | 1.00 |
drug2122 | Placebo Wiki | 0.05 |
Name (Synonyms) | Correlation | |
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D003141 | Communicable Diseases NIH | 0.08 |
D007239 | Infection NIH | 0.05 |
D045169 | Severe Acute Respiratory Syndrome NIH | 0.05 |
D018352 | Coronavirus Infections NIH | 0.04 |
Name (Synonyms) | Correlation |
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There is one clinical trial.
The purpose of this study is to explore the effectiveness of processed human amniotic fluid as a treatment for COVID-19.
Description: Assess reduction of inflammation in COVID-19 patients, potentially leading to a decrease in the need for critical care. This will be assessed by measurement of C-reactive protein levels before and after the intervention. Units: mg/dL
Measure: C-reactive protein Time: Baseline through post-treatment (6 days)Description: Comparison of mortality between intervention and control groups
Measure: Death within 30 Days Time: Baseline through 30 daysDescription: Comparison of days spend in ICU between intervention and control groups
Measure: ICU-free days at 30 days Time: Baseline through 30 daysDescription: Comparison of days spent in hospital between intervention and control groups
Measure: Hospital length of stay Time: From date of hospital admission through date of discharge or death, whichever comes first (up to 100 days)Description: Comparison of mechanical ventilation incidence between intervention and control groups
Measure: Need for invasive mechanical ventilation Time: From date of enrollment through date of discharge or death, whichever comes first (up to 100 days)Description: Comparison of mean biomarker level change between intervention and control groups. Units: pg/mL
Measure: Biomarker levels (interleukin-6) Time: Baseline through post-treatment (6 days)Description: Comparison of mean biomarker level change between intervention and control groups. Units: ug/mL
Measure: Biomarker levels (d-dimer) Time: Baseline through post-treatment (6 days)Description: Comparison of mean biomarker level change between intervention and control groups. Units: u/L
Measure: Biomarker levels (lactate dehydrogenase) Time: Baseline through post-treatment (6 days)Description: Comparison of ECMO incidence between intervention and control groups
Measure: Need for ECMO Time: From date of enrollment through date of discharge or death, whichever comes first (up to 100 days)Description: Compare frequency of major adverse cardiac events (MACE) between intervention and control groups
Measure: Major adverse cardiac events Time: From date of enrollment through date of discharge or death, whichever comes first (up to 100 days)Description: Comparison of PROMIS (Patient-Reported Outcomes Measurement Information System) questionnaire results on a computer-adaptive platform between intervention and control groups using T-scores. Scale mean = 50, standard deviation = 10.
Measure: Patient-reported functional status Time: Administered at 1, 3, 6, and 12 months post discharge (1 year)Description: Patients will be administered a 20-question self-report measure of PTSD symptoms. Total scores range from 0-80. Scores of 31-33 or above generally indicate clinically likely PTSD.
Measure: PTSD Checklist Time: Administered at 1, 3, 6, and 12 months post discharge (1 year)