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Multi-hospital, exploratory clinical trial for evaluating the efficacy and safety of edema relief and leg pain reduction effect in the treatment using Intermittent pneumatic Compression for patients with edema pain in daily life

Not Applicable
Recruiting
Conditions
Endocrine, nutritional and metabolic disease
Registration Number
KCT0004562
Lead Sponsor
Presbyterian Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
5
Inclusion Criteria

1) Adult men and women over 19 years old
2) Those who have leg pain due to edema in their daily life
3) A person who fully understands the purpose and procedure of the research and wishes to participate in the clinical research through voluntary consent.

Exclusion Criteria

1) Those who do not meet the age standard
2) Those who complain of numbness
3) Those who have had lower extremity surgery within the last 6 months
4) The person in charge who deems it inappropriate for participation in the test

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale
Secondary Outcome Measures
NameTimeMethod
eg volume;Leg circumference
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