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BiPAP for Cardiomyopathy With Central Sleep Apnea

Primary Purpose

Dilated Cardiomyopathy

Status
Completed
Phase
Not Applicable
Locations
Japan
Study Type
Interventional
Intervention
bilevel positive airway pressure
bilevel positive airway pressure (Device)
Sponsored by
Nagoya University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dilated Cardiomyopathy

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Idiopathic dilated cardiomyopathy Exclusion Criteria: a history of alcohol abuse, diabetes mellitus, endocrine disorders, hypertension, obstructive sleep apnea syndrome, and chronic obstructive pulmonary disease

Sites / Locations

  • Nagoya University of Health Sciences

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 26, 2006
Last Updated
January 27, 2006
Sponsor
Nagoya University
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1. Study Identification

Unique Protocol Identification Number
NCT00282789
Brief Title
BiPAP for Cardiomyopathy With Central Sleep Apnea
Study Type
Interventional

2. Study Status

Record Verification Date
June 2000
Overall Recruitment Status
Completed
Study Start Date
June 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Nagoya University

4. Oversight

5. Study Description

Brief Summary
We investigated whether treatment of central sleep apnea-hypopnea with bilevel positive airway pressure (BiPAP) in patients with idiopathic dilated cardiomyopathy (IDCM) would improve LV function.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dilated Cardiomyopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
bilevel positive airway pressure
Intervention Type
Device
Intervention Name(s)
bilevel positive airway pressure (Device)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Idiopathic dilated cardiomyopathy Exclusion Criteria: a history of alcohol abuse, diabetes mellitus, endocrine disorders, hypertension, obstructive sleep apnea syndrome, and chronic obstructive pulmonary disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mitsuhiro Yokota, MD,PhD
Organizational Affiliation
Department of Cardiovascular Genome Science, Nagoya University School of Medicine, Nagoya, Aichi, Japan
Official's Role
Study Chair
Facility Information:
Facility Name
Nagoya University of Health Sciences
City
Nagoya
ZIP/Postal Code
461-8673
Country
Japan

12. IPD Sharing Statement

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BiPAP for Cardiomyopathy With Central Sleep Apnea

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