Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV) (NCT06240637) | Clinical Trial Compass
RecruitingNot Applicable
Telemonitoring Utility in the Process of Adaptation to Home Mechanical Ventilation (HMV)
Spain48 participantsStarted 2024-02-17
Plain-language 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
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
What they're measuring
1
Measurement of pCO2 by arterial blood gas
Timeframe: 6 months
Trial details
NCT IDNCT06240637
SponsorFundaciĆ³ Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau