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sefulness of compression stockings for nocturia

Not Applicable
Conditions
octuria
Registration Number
JPRN-UMIN000047192
Lead Sponsor
Dokkyo Medical University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
34
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with hypersensitivity to compression stocking material Patients deemed inappropriate for this study by the principal investigator Patients who have refused to participate in this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Amount of change in nocturnal urination frequency in frequency volume chart
Secondary Outcome Measures
NameTimeMethod
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