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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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004562
Enrollment
5
Registered
2019-12-18
Start date
2019-12-05
Completion date
Unknown
Last updated
2020-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : 1. Clinical Trial Equipment: Intermittent Pneumatic Compression Device 2. Treatment: Study subjects perform three treatments per visit. - Natual mode : 60 minutes rest after visit - W

Sponsors

Presbyterian Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale—

Secondary

MeasureTime frame
Leg volume;Leg circumference—

Countries

Korea, Republic of

Contacts

Public ContactSeung-Rok Kang

Chonbuk National University Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026