A clinical study of explore wearable applicability of low-power irradiator for knee joint pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009377

Enrollment

Registered

2024-04-26

Start date

2024-04-03

Completion date

Unknown

Last updated

2024-04-29

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 : 6 people to the control group (a group in which a low-power irradiator was applied for 15 minutes) after the test group (a group in which a low-power irradiator was applied for 120 mi

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients aged between 19 and 64 years old 2. Those who agree to participate in this study and voluntarily sign this study 3. Those whose VAS(visual analog scale) of knee joint pain is 40 or higher

Exclusion criteria

Exclusion criteria: 1. Those who have skin allergies or abnormal reactions to sunlight 2. Those with other chronic diseases (stroke, myocardial infarction, kidney disease, diabetic neuropathy, dementia, epilepsy, etc.) that may interfere with the treatment effect or interpretation of results. 3. Those who have a skin wound on the affected knee and are at risk of infection 4. Patients with malignant tumors (can participate if no recurrence occurs within 5 years after completion of treatment) 5. Those currently taking steroids (prednisolone, methylprednisolone, betamethasone, dexamethasone, hydrocortisone, etc.), immunosuppressants (calcineurin inhibitors (cycloproline, tacrolimus), mTOR inhibitors (sharolimus, everolimus), antimetabolites (mycophenolate), drugs for mental illness (antidepressants (lorazepam, alprazolam, sertraline), anti-anxiety drugs (benzodiazepines, buspirone), etc.) or other drugs that may affect the results of the study. 6. Those who have participated in clinical trials for the treatment of knee joint pain within the past 3 months 7. Pregnant or breastfeeding 8. Those who participated in another clinical study and received intervention within 4 weeks of the screening visit of this study 9. Those who have difficulty filling out the consent form to participate in research 10. Other people who, in the opinion of the researcher, find it difficult to participate in clinical research 11. Those who have had knee surgery within 3 months

Design outcomes

Primary

Measure	Time frame
Knee joint pain VAS(Visual Analogue Scale)	—

Secondary

Measure	Time frame
Western Ontario and McMaster Universities Index;EuroQoL 5-Dimension 5-Level;Convenience evaluation	—

Countries

Korea, Republic of

Contacts

Public ContactJae-hui Kang

Cheonan Korean Medicine Hospital of Daejeon University

rkd12@hanmail.net+82-41-521-7579

Outcome results