UnknownNot Applicable

Telemonitoring in Home Mechanical Ventilation

Belgium20 participantsStarted 2024-01-01

Plain-language summary

Multicentric, observational and longitudinal prospective evaluation of build-in-software data telemonitoring of home ventilators in patients using Home Mechanical Ventilation in Belgium.

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: * All patients starting HMV in 2024, followed up in 1/ Liège or 2/ Brussels, and using devices from the ResMed company (Astral 150 ou Lumis 150). Exclusion Criteria: * Individuals refusing to sign the consent form * Presence of acute pathology requiring hospitalization and close monitoring of ventilation * Patients using a tracheostomy

What they're measuring

Compliance to the treatment

Timeframe: T1: Mean value during night 1 (inpatient)

Compliance to the treatment

Timeframe: T2: Mean value during night 2 (inpatient)

Compliance to the treatment

Timeframe: T3: Mean value during nights 24-30 (outpatient)

Compliance to the treatment

Timeframe: T4: Mean value during nights 174-180 (outpatient)

Leaks

Timeframe: T1: Median value during night 1 (inpatient)

Leaks

Timeframe: T2: Median value during nights 2 (inpatient)

Leaks

Timeframe: T3: Median value during nights 24-30 (outpatient)

Leaks

Timeframe: T4: Median value during nights 174-180 (outpatient)

Trial details

NCT IDNCT06143384

SponsorErasme University Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-01-01

Contact for this trial

Michel Toussaint, PhD

+322555 67 54 michel.toussaint@hubruxelles.be

View on ClinicalTrials.gov More Respiratory Insufficiency Requiring Mechanical Ventilation trials