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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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006449
Enrollment
20
Registered
2021-08-13
Start date
2021-05-27
Completion date
Unknown
Last updated
2021-08-30

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 : Stimulation: (Control group) High-frequency stimulation with minimum output using the same type of high-frequency minimum output device, (Experimental group) High-frequency stimulati

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale

Secondary

MeasureTime frame
ultrasound test(plantar fascia thickness and fat pad thickness);The American Orthopedic Foot and Ankle Society-ankle-hindfoot scale;foot function index

Countries

Korea, Republic of

Contacts

Public ContactSeung-Rok Kang

Jeonbuk National University Hospital

srkang@mdctc.or.kr+82-63-259-3458

Outcome results

None listed

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