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RECRUITING
NCT06952816
NA

Validation Study of the EMILY AI Device in Acute and Chronic Respiratory Failure

Sponsor: Aether Tech S.L.

View on ClinicalTrials.gov

Summary

Currently, there is no holistic solution for patients with respiratory diseases that includes oxygenation and management of a patient with respiratory disease, combining dynamic and automatic O2 administration and the detection of clinical worsening, generating a diagnostic suspicion, a management proposal, and notifying the medical team. For device validation, prospective studies will be conducted in patients in respiratory intermediate care units, conventional hospitalization, during physical activity in the hospital setting, and in an out-of-hospital setting. The device will be evaluated in terms of oxygenation efficacy, response time, patient safety, efficiency, versatility, clinical benefit, and adaptability.

Official title: Functional, Clinical, and Predictive Validation Study of the EMILY AI Device in Patients With Acute and Chronic Respiratory Failure

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2025-04-23

Completion Date

2026-12-30

Last Updated

2026-01-09

Healthy Volunteers

No

Interventions

DEVICE

Emily.AI

EMILY.AI is composed of an O2 regulating valve together with an intelligent system which allows the automation in the regulation of O2 and its customization.

Locations (2)

Hospital Universitario Fundación Jiménez Díaz

Madrid, Spain

Hospital Universitario Fundación Jiménez Díaz

Madrid, Spain