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

Recruiting now · Not applicable

Conditions studied: Non Invasive Ventilation

In brief

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).

Key facts

Study ID

NCT06240637

Run by

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

People needed

48

Starts

2024-02-17

Expected to finish

2026-12-01

Last updated by the study team

2024-03-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Chronic hypercapnic respiratory failure with indication for home mechanical ventilation.
• Patients who require ventilation with spontaneous-timed mode.
• Signing of informed consent.

You may not qualify if…

• 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

Where it is running

• Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau — Barcelona, Spain (enrolling)

Full record on ClinicalTrials.gov

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