Monitoring of Patients With Chronic Respiratory Failure Treated With Non-invasive Home Ventilation: Contribution of New Monitoring Tools

NCT ID: NCT04872062

Last Updated: 2021-05-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-11-01

Study Completion Date

2021-05-31

Brief Summary

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Single-center retrospective study conducted on a population of patients with chronic hypercapnic respiratory failure treated by non-invasive ventilation at home, followed at the CHRU of Nancy. The objective is to assess the contribution of reading the NIV card with a standardized grid in their follow-up. The main objective is to assess the inter-observer agreement of a standardized NIV card reading grid, the secondary objective is to compare the results of NIV card reading between the usual NIV card reading method in the service and this same method completed by the addition of the standardized reading grid. The hypothesis is that the use of a standardized NIV card reading grid improves patient follow-up by standardizing their care.

Detailed Description

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Conditions

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Chronic Hypercapnic Respiratory Failure

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Chronic hypercapnic respiratory failure treated by home non-invasive ventilation (NIV)

NIV cards

Intervention Type DEVICE

Reading the data available on the NIV cards

Medical file

Intervention Type OTHER

Using the data available in the medical file including clinical data, blood gas results, nocturnal oximetry results

Interventions

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NIV cards

Reading the data available on the NIV cards

Intervention Type DEVICE

Medical file

Using the data available in the medical file including clinical data, blood gas results, nocturnal oximetry results

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Major patients
* Patients with chronic hypercapnic respiratory failure with a validated indication of long-term NIV
* Follow-up at the CHRU of Nancy at "Unité de Médecine Ambulatoire" (UMA) department between 11/01/2020 and 05/30/2021

Exclusion Criteria

* Data not usable / missing
* Tracheal ventilation
* Patients' opposition to the use of their data for the purposes of this research
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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SOLER Julien

Hospital practitioner

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Julien Soler

Role: STUDY_DIRECTOR

CentraHNF

Locations

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CHRU de Nancy - Site de Brabois

Nancy, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Julien Soler

Role: CONTACT

+33647961454

Facility Contacts

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Julien Soler

Role: primary

+33647961454

Other Identifiers

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2020PI282

Identifier Type: -

Identifier Source: org_study_id

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