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Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV)

Non Invasive Ventilation Clinical Trial

Official title:
Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation

Clinical Trial Summary

The goal of this clinical trial is to evaluate whether telemonitoring, added to the usual process of adaptation to home mechanical ventilation (HMV), achieves a more efficient correction of hypoventilation (reduction of hypercapnia).

Clinical Trial Description

The study population consist of patients with hypercapnic respiratory failure eligible for Home Mechanical Ventilation (HMV) with a total of 48 subjects (24 per group). In those patients with hypercapnic respiratory failure who have an indication for home mechanical ventilation (HMV), without criteria for life support, the initial titration will be performed following the protocol of the Pulmonology Service. After their education, patients will be randomized into one of the following groups: the control group and the telemonitoring group with daily review of Home Mechanical Ventilation (HMV) data. The objectives are to evaluate whether hypoventilation is corrected more efficiently, compare treatment adherence between both groups, analyze unforeseen visits, and assess the number of hospital admissions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06240637
Study type Interventional
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact
Status Recruiting
Phase N/A
Start date February 17, 2024
Completion date December 1, 2026
View Details
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