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Effectiveness of Adaptive Servo-Ventilation for severe aortic stenosis patients after aortic valve replacement

Not Applicable
Conditions
severe aortic stenosis
Registration Number
JPRN-UMIN000021139
Lead Sponsor
Osaka university hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

(1) patients who will undergo the other valve surgery (2) patients who have chronic Af before surgery (3) patients who will undergo MAZE procedure (4) patients who are complicated with central sleep apnea rather than obstructive sleep apnea (5) Patients who are considered unsuitable to participate in the study than the researcher because of other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
YHA, 6-minute walk, Specific Activity Scale (24 weeks)
Secondary Outcome Measures
NameTimeMethod
BNP, Dd, FS, EF, LVM (12, 24 weeks)
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