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NOT YET RECRUITING
NCT06637800
NA

Prospective, Open-label Study of Seraph 100 in Patients With Prolonged COVID (PC)

Sponsor: ExThera Medical Corporation

View on ClinicalTrials.gov

Summary

This study will use a prospective, open, single-arm design, in which a group of 100 patients with a diagnosis of prolonged COVID, previously selected according to inclusion and exclusion criteria, and who have undergone informed consent process and have signed the informed consent form, undergo two hemoperfusion procedures with the Seraph 100 filter, on consecutive days. They are then evaluated at day 3 and 4 weeks, to complete the safety and effectiveness assessment.

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2025-02-15

Completion Date

2025-04

Last Updated

2025-01-24

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Seraph® 100 Microbind® Affinity Blood Filter (Seraph 100)

The Seraph 100 is part of the Seraph platform technology that was developed as an extracorporeal broad-spectrum sorbent hemoperfusion device for reduction of pathogens, bacteria, viruses, fungus, and other sepsis mediators from the bloodstream. In addition, it has been demonstrated that Seraph 100 is also capable of removing circulating tumor cells from the whole blood.

Locations (1)

Hospital Angeles Tijuana

Tijuana, Mexico