Clinical Trials Directory

Trials / Unknown

UnknownNCT04317469

Evaluation of Von Willebrand Factor as a Marker For Early Diagnosis of Acute Respiratory Distress Syndrome (A.R.D.S) in Comparison to Interleukin 6 [IL-6]

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

In this prospective study of 60patients, we tested the hypothesis That markedly elevated levels of plasma von Willebrand factor (VWF) a marker of endothelial cell injury might predict the development of acute respiratory distress syndrome (A.R.D.S) in risky patients. We compared our result to IL.6 as control biomarker for A.R.D.S development. Acute lung injury was quantified on two -point scoring system (Berlin definition of ARDS and Murray score of acute lung injury). Plasma levels of both vWF and IL.6 were be measured on T=0 i.e. (at start of the study once the patient considered to be risky for A.R.D.S development to obtain their baseline levels), T=48 (after 48 hours), and T=72 (after 72 hours).

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVWF measurementPlasma levels of both vWF and IL.6 were be measured on T=0 i.e. (at start of the study once the patient considered to be risky for A.R.D.S development to obtain their baseline levels), T=48 (after 48 hours), and T=72 (after 72 hours).

Timeline

Start date
2020-03-21
Primary completion
2021-03-20
Completion
2021-09-20
First posted
2020-03-23
Last updated
2020-03-23

Source: ClinicalTrials.gov record NCT04317469. Inclusion in this directory is not an endorsement.