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Clinical trial on pain relief and improvement of foot function when applied to patients with plantar pain using HIPER-500TM, a high-frequency stimulator

Not Applicable
Recruiting
Conditions
Symptoms, signs and abnormal clinical and laboratory findings, NEC
Registration Number
KCT0006449
Lead Sponsor
Jeonbuk National University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

1) Adult men and women over the age of 20
2) Those who have pain in the soles of the feet during activities of daily living
3) Those who have tenderness in the calcaneus during physical examination
4) A person who can express his or her opinion and can perform instructions

Exclusion Criteria

1) Those who are suspected of having symptoms such as ankle and toe bone fractures including calcaneus, lumbar neuropathy, and ankle ligament injury
2) Those with a history of treatment for plantar fascitis within 3 months
3) Those with a history of foot or ankle-related surgery in the last 6 months
4) Persons with cognitive or behavioral disorders that are difficult to perform
5) Those who cannot detect temperature changes
6) Those with malignant tumors or skin diseases
7) Acute disease patients, high fever patients, people with heart problems, and those who insert metal-type aids into body parts (bones, legs, feet, waist, etc.)
8) Persons whose intentions are not clear (children, the disabled, the elderly, etc.)
9) Others recognized by the principal investigator as inappropriate to participate in the study

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale
Secondary Outcome Measures
NameTimeMethod
ultrasound test(plantar fascia thickness and fat pad thickness);The American Orthopedic Foot and Ankle Society-ankle-hindfoot scale;foot function index
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