Covid19 Clinical Trial - Mask Adhesive Institutional Study

Status Terminated

Clinical Trial Summary

To reduce interface leak and aerosol spread, Philips has developed an accessory to non-invasive ventilation(NIV) masks to be used with the Philips AF531 and the PerformaTrak mask on respiratory failure patients. For the purposes of capturing initial mask leak and safety data, this trial will enroll patients treated with NIV in an institutional setting (i.e., sleep lab).

Clinical Trial Description

The Mask Adhesive will serve as an accessory to the AF531/PerformaTrak masks with the intention to reduce patient leak while a patient is receiving therapy. This accessory is a double-sided adhesive; with one side applied directly to the patient's skin and the other side connected to the mask cushion. Each adhesive is only to be applied to a patient once. The AF531/Performatrak mask can be removed from the adhesive and then re-applied, as necessary. For example, if the patient needs to remove the mask to eat or take medicine, the mask is removed from the patient and the adhesive will stay on the patient's face ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04644276
Study type	Interventional
Source	Philips Clinical & Medical Affairs Global
Contact
Status	Terminated
Phase	N/A
Start date	February 17, 2021
Completion date	December 9, 2021

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