Prognosis in Patients With Chronic Respiratory Failure Receiving Domiciliary Noninvasive Positive Pressure Ventilation (NPPV)

NCT ID: NCT00905476

Last Updated: 2015-04-03

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

COMPLETED

Total Enrollment

56 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-04-30

Study Completion Date

2014-11-30

Brief Summary

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The purposes of the present study are (1) to analyze baseline patient characteristics cross-sectionally, (2) to analyze the prognosis and its predictive factors, and (3) to examine longitudinal clinical course in patients with chronic respiratory failure receiving domiciliary NPPV.

Detailed Description

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Limited data are available about the prognosis and its predictive factors in patients with chronic respiratory failure receiving domiciliary NPPV. In addition, their health status, psychological status and sleep quality seem to be highly disturbed due to severe respiratory insufficiency. Therefore, in the present study, we aim to examine (1) contributive factors to health status based on baseline data, (2) whether patient reported measurements such as health status, dyspnea and psychological status would predict patient's future outcomes, and (3) how they would change for 3 years as compared to physiological measurements.

Conditions

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Chronic Respiratory Failure

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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NPPV

Patients with chronic respiratory failure receiving domiciliary NPPV

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients with chronic respiratory failure receiving domiciliary NPPV for more than 3 months

Exclusion Criteria

* Uncontrolled severe comorbidities
* Patients with tracheotomy.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry of Health, Labour and Welfare, Japan

OTHER_GOV

Sponsor Role collaborator

Kyoto University, Graduate School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Toru Oga

Respiratory Care and Sleep Control Medicine, Kyoto University, Graduate School of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kazuo Chin, M.D.

Role: STUDY_CHAIR

Graduate School of Medicine, Kyoto University

Locations

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NHO Minami-Kyoto Hospital

Jōyō, , Japan

Site Status

Kobe City Hospital Organization Medical Center West Hospital

Kobe, , Japan

Site Status

Kobe City Medical Center General Hospital

Kobe, , Japan

Site Status

Komaki Municipal Hospital

Komaki, , Japan

Site Status

Graduate School of Medicine, Kyoto University

Kyoto, , Japan

Site Status

Ogaki Municipal Hospital

Ōgaki, , Japan

Site Status

Otsu Red Cross Hospital

Ōtsu, , Japan

Site Status

Tosei General Hospital

Seto, , Japan

Site Status

Takatsuki Red Cross Hospital

Takatsuki, , Japan

Site Status

Tenri Hospital

Tenri, , Japan

Site Status

NHO Toneyama National Hospital

Toyonaka, , Japan

Site Status

Countries

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Japan

References

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Oga T, Taniguchi H, Kita H, Tsuboi T, Tomii K, Ando M, Kojima E, Tomioka H, Taguchi Y, Kaji Y, Maekura R, Hiraga T, Sakai N, Kimura T, Mishima M, Windisch W, Chin K. Comparison of Different Disease-Specific Health-Related Quality of Life Measurements in Patients with Long-Term Noninvasive Ventilation. Can Respir J. 2017;2017:8295079. doi: 10.1155/2017/8295079. Epub 2017 May 15.

Reference Type DERIVED
PMID: 28588383 (View on PubMed)

Other Identifiers

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E552kyoto

Identifier Type: -

Identifier Source: org_study_id

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