CovidResearchTrials by Shray Alag


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ARFC maskWiki

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


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug2729 acute kidney injury Wiki 1.00

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D058186 Acute Kidney Injury NIH 0.24

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0001919 Acute kidney injury HPO 0.24

There is one clinical trial.

Clinical Trials


1 Evaluation of ARFC Masks Equipped With CF5 Filter in the Care Unit to Allow a Wider Distribution of FFP2 Masks (Covid-19).

The current outbreak of Covid-19 requires the wearing of FFP2 respiratory protective devices by healthcare personnel to limit their contamination. However, there is currently a shortage of masks in France due to insufficient national stocks while the disease is spreading. There is an urgent need to save FFP2 masks to enable healthcare personnel to continue to provide care in complete safety. Contamination of staff due to insufficient masks would have consequences by limiting access to care for infected patients and putting caregivers at potential risk of death. Caregiver protection is also intended to contain the risk of nosocomial epidemics. We propose the use of ARFC masks by Covid-19+ units. These ARFC masks provide optimal security against the risk of aerosolization of contaminated biological liquids. They are masks modified to be usable by civilians, resulting from the technology of combat masks, specially designed for use in NRBC (Nuclear, Radiological, Biological and Chemical) atmosphere.

NCT04427176 Nurse Device: ARFC mask

Primary Outcomes

Description: Tolerance will be assessed by the nursing staff by means of a visual analogue scale from 0: no tolerance to 10: perfect tolerance. It will be evaluated 48 hours after the inclusion.

Measure: Evaluate the feasibility of the use of an ARFC mask by nursing staff, in terms of tolerance

Time: Hour: 48

Description: Compatibility will be assessed by the number of catheter insertion and blood sampling failures in relation to the total number of catheter insertions and blood sampling indicated at 48 hours after the inclusion.

Measure: Evaluate the feasibility of the use of an ARFC mask by nursing staff, in terms of compatibility with technical gestures.

Time: Hour: 48

Secondary Outcomes

Description: To compare acceptability questionnaires complete at inclusion and 48 jours after.

Measure: Assess the acceptability of the wearing of an ARFC mask by nursing staff

Time: Hours: 0, 48

Description: Occurrence of minor complications related to the wearing of the mask as reported for non-invasive ventilation (dry mouth, nose, conjunctivitis, skin lesions at the support point, etc.).

Measure: To assess the minor complications of wearing the ARFC mask .

Time: Hour: 48


No related HPO nodes (Using clinical trials)