CovidResearchTrials by Shray Alag


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Human Amniotic FluidWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug254 ArtemiC Wiki 1.00
drug2122 Placebo Wiki 0.05

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
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

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Phase I/II Randomized Double-blinded Placebo-controlled Clinical Trial to Determine Safety and Feasibility of Using an Acellular Sterile Filtered Amniotic Fluid as a Treatment for COVID-19 Patients

The purpose of this study is to explore the effectiveness of processed human amniotic fluid as a treatment for COVID-19.

NCT04497389 SARS CoV-2 Biological: Human Amniotic Fluid

Primary Outcomes

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)

Other Outcomes

Description: Comparison of mortality between intervention and control groups

Measure: Death within 30 Days

Time: Baseline through 30 days

Description: Comparison of days spend in ICU between intervention and control groups

Measure: ICU-free days at 30 days

Time: Baseline through 30 days

Description: 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)


No related HPO nodes (Using clinical trials)