Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV)
Trial Parameters
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Brief 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).
Eligibility Criteria
Inclusion Criteria: * Chronic hypercapnic respiratory failure with indication for home mechanical ventilation. * Patients who require ventilation with spontaneous-timed mode. * Signing of informed consent. Exclusion Criteria: * Patient already treated with mechanical ventilation or home CPAP. * Patient requiring mechanical ventilation as life support. * Pregnancy. * Cognitive impairment that makes it impossible to understand the informed consent for the study. * Psychiatric pathology that makes compliance with therapy or its follow-up difficult. * Impossibility of complying with the protocol. * Expected survival less than 12 months. * Any other condition that, in the opinion of the researcher, could interfere with the objectives of the study