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Short-term Effects of Humidification Devices on Respiratory Pattern and Work of Breathing During Invasive Ventilation

Short-term Effects of Humidification Devices on Respiratory Pattern and Work of Breathing During Invasive Ventilation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02499796
Enrollment
15
Registered
2015-07-16
Start date
2015-04-30
Completion date
2015-09-30
Last updated
2018-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Respiratory Failure

Keywords

Invasive mechanical ventilation, Humidifying devices, Respiratory mechanics

Brief summary

This study compares the short-term effects of a new humidification system (Hygrovent Gold) and two other humidification devices (heated and moisture exchanger and heated humidifier) on respiratory pattern and work of breathing, during invasive ventilation.

Detailed description

Three humidifying devices are commonly and indifferently used during mechanical ventilation, but their impact on respiratory mechanics and, eventually, mechanical ventilation efficacy, particularly in patients highly dependent from mechanical ventilation, are not superimposable. It has already been described that heated and moisture exchangers (HME), increasing dead space, can negatively affect ventilatory function and gas exchange, in comparison to heated humidifiers (HH). The Hygrovent Gold, mainly because of its position between the tracheostomy and the Y-piece of the ventilatory circuit and its structure, may lead to analogous or even worse effects, determining and increase in inspiratory resistances and dead space and consequently an increase in the work of breathing.

Interventions

DEVICEHygrovent Gold
DEVICEHeated and moisture exchanger (HME)
DEVICEHeated humidifier (HH)

Sponsors

Fondazione Salvatore Maugeri
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic hypercapnic respiratory failure (PaCO2 of 45 mmHg or more) * Long-term mechanical ventilation via tracheostomy * Clinical stability

Exclusion criteria

* Non collaborative subjects * Acute respiratory failure * Haemodynamic instability * Encephalopathy

Design outcomes

Primary

MeasureTime frame
Change in muscle pressure-time product (PTPoes)Baseline and 60 minutes

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026