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CPAP and NIV Interfaces : Side-effects in Home Care Patients

Descriptional Study of the Side Effects Related to the Use of the Interface in Home Care Patients Treated for at Least 3 Months by Continuous Positive Pressure or Non-Invasive Ventilation.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03013283
Acronym
InterfaceVent
Enrollment
6000
Registered
2017-01-06
Start date
2017-02-07
Completion date
2019-04-01
Last updated
2021-01-27

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

Conditions

Continuous Positive Airway Pressure (CPAP), Hyperventilation Anxiety, Interface, Mask, Non Invasive Ventilation (NIV), Sleep Apnea Syndrome (OSAS)

Brief summary

Home ventilation techniques consist mainly of two techniques, Continuous Positive Airway Pressure or CPAP and Non Invasive Ventilation or NIV. Whether for CPAP or NIV, pressures are delivered to the patient via an interface. The efficacy of CPAP and NIV is conditioned in part by the observance of the patients to the device. Because the comfort and degree of satisfaction of the patients to its interface is a key factor of the observance, side-effects and satisfaction of patients need to be continuously evaluated with available interfaces for CPAP and NIV treated patients. The purpose of the research is the evaluation of interface side-effects and the degree of satisfaction of home care patients treated for at least three months with CPAP or NIV.

Detailed description

Home ventilation techniques consist mainly of two techniques, Continuous Positive Airway Pressure or CPAP (the level of pressure delivered being constant) and Non Invasive Ventilation or NIV (pressure level varies from an expiratory pressure to an inspiratory pressure). Whether for CPAP or NIV, pressures are delivered to the patient via an interface. Many manufacturers produce interfaces and these interfaces are the subject of regular technological innovations with the introduction on the market of new product ranges. Because of the lack of dedicated and actualized studies, there is poor evidence based of difference between old and new interfaces, there is also poor evidence based of differences between manufacturer products. The efficacy of CPAP and NIV is conditioned in part by the observance of the patients to the device. Because the comfort and degree of satisfaction of the patients to its interface is a key factor of the observance, side-effects and satisfaction of patients need to be continuously evaluated with available interfaces for CPAP and NIV treated patients. The purpose of the research is the evaluation of interface side-effects and the degree of satisfaction of home care patients treated for at least three months with CPAP or NIV. A visual analog scale is used to assess the patient perception of its interface. A measure of the quality of life and a home care technician evaluation are performed simultaneously. Using the device manufacturer software, a measure of the observance, level of pressure and leak is realised. A first intermediate analysis will be made after approximately 1000 inclusions (the Sleepileaks (determinants of residual excessive sleapiness), Threshleaks (high leak levels and machine adherence as defined by the American Thoracic Society) and Complileaks studies (all leaks and machine adherence as continuous variables)). A second validating analysis will be made at the end of inclusions.

Interventions

* Interface side effects and degree of satisfaction of the patients * Technician evaluation and device measures.

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Written informed consent * Age more than 18 years (inclusive) * Patient treated with CPAP or NIV for at least three months,and eligible for care and for the reimbursement by the French Social Security rules. * Patient presents during a scheduled home visit of the technician for the continuation of CPAP or NIV treatment according to the French Social Security rules.

Exclusion criteria

* Pregnancy, intention of being pregnant, breastfeeding. * Inability to understand the nature and aims of the study or to communicate with the investigator * Simultaneous participation in another trial with an exclusion clause to participate to an other trial. * No affiliation to the French social security * Loss of personal capacity resulting in state protection * Deprivation of liberty by judicial or administrative decision

Design outcomes

Primary

MeasureTime frameDescription
Interface side effects and degree of satisfaction of the patients1 dayDuring a scheduled home visit of the technician. The primary endpoint is a composite criterion corresponding to the patients' responses to a self-administered questionnaire.

Secondary

MeasureTime frameDescription
Percentage of patients with oxygen therapy, heated humidifier, chinstrap.1 dayDuring a scheduled home visit of the technician : Percentage of patients with oxygen therapy, heated humidifier, chinstrap.
Collection by technician of the type of interface1 dayDuring a scheduled home visit of the technician : Collection by technician of the type of interface (nasal pillows, nasal and oronasal, custom made interface), manufacturer name and interface size, type (CPAP/NIV) and manufacturer name of the device.
Compliance1 dayDuring a scheduled home visit of the technician : Device software data: compliance (hour per day) over the last 3 months
Average level of intentional or unintentional leakage1 dayDuring a scheduled home visit of the technician : Device software data: average level of intentional or unintentional leakage (l/min)
Residual AHI1 dayDuring a scheduled home visit of the technician : Device software data: residual AHI (event/hour)
Average pressure level and pressure1 dayDuring a scheduled home visit of the technician :Device software data: average pressure level and pressure at the 90/95th percentile (cmH2O).
Identification by the technician of the problems of pain1 dayDuring a scheduled home visit of the technician : Identification by the technician of the problems of pain, erythema and leak, localization of these problems.
Date of first installation of the first ventilation device1 dayDate of first installation of the first ventilation device
Proportion of patient responding to self-help questionnaire without assistance1 dayProportion of patient responding to self-help questionnaire without assistance
Proportion of patients able to position the interface without assistance1 dayProportion of patients able to position the interface without assistance
Time taken by the patient and the technician to answer the patient's self-questionnaire and the technician record respectively.1 dayTime taken by the patient and the technician to answer the patient's self-questionnaire and the technician record respectively.
Proportion of patient waiting for a new interface1 dayProportion of patient waiting for a new interface
Proportion of patients wishing to participate in research on the subject.1 dayProportion of patients wishing to participate in research on the subject.
Patient quality of life questionnaire1 dayPatient quality of life questionnaire (EQ-5D 3L, Epworth).

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026