Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV)
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).
| Condition(s) | Non Invasive Ventilation |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| 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). |
| Who can participate | 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 |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau |
| Locations | Barcelona, Spain |
| Start date | 2024-02-17 |
| NCT ID | NCT06240637 |
| Official listing | https://clinicaltrials.gov/study/NCT06240637 |