Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV)
Recruiting
N/A
Interventional Study
Non Invasive Ventilation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 48 (estimated)
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · Other
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About This Trial
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).
Trial Locations
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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.
* P…
Contacts
No contact information available.