Status:
RECRUITING
The Effectiveness and Safety of Pharmacopuncture on Inpatients With Acute Knee Pain Caused by Traffic Accidents
Lead Sponsor:
Jaseng Medical Foundation
Conditions:
Pharmacologic Action
Eligibility:
All Genders
19-69 years
Phase:
NA
Brief Summary
The purpose of this study is to reveal the effectiveness and safety of knee herbal acupuncture for patients with acute knee joint pain caused by a traffic accident. It is a practical clinical study to...
Eligibility Criteria
Inclusion
- When the NRS (Numeric Rating Scale) of knee pain caused by a traffic accident is 5 or higher.
- Patients hospitalized for traffic accident treatment.
- Patients with acute pain within 14 days of experiencing knee pain due to a traffic accident.
- Patients aged between 19 and 70 years old.
- participants who agree to participate in clinical research and provide written test subject consent.
Exclusion
- For patients diagnosed with a specific serious disease that may cause knee pain (acute fracture, dislocation, complete rupture of ligaments, etc.)
- If the cause of the pain is caused by a disease other than the knee (tumor, fibromyalgia, rheumatoid arthritis, gout, lumbar disc herniation, etc.)
- Cases where surgical intervention is required due to suspected acute fracture, dislocation, or ligament and cartilage damage
- If there is another acute disease (stroke, myocardial infarction, kidney disease, diabetic neuropathy, dementia, epilepsy, etc.) that may interfere with the treatment effect or interpretation of results
- Patients currently taking steroids, immunosuppressants, mental illness drugs, or other drugs that may affect their findings
- Inadequate or unsafe medication: hemorrhagic disease, anticoagulant therapy, severe diabetic patients with risk of infection
- Patients who have taken drugs that may affect pain, such as Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), or have received herbal acupuncture or physical therapy within the past week
- In the case of pregnant women and in the case of planning to become pregnant or nursing
- Patients within 3 months after knee surgery or if knee replacement surgery was performed
- If it has been less than 1 month since participants finished participating in another clinical study, or if participants are planning to participate in another clinical study during the study participation and follow-up period within 6 months from the date of selection
- If it is difficult to fill out the consent form for research participation
- In cases where it is difficult for other researchers to participate in clinical research
Key Trial Info
Start Date :
May 22 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT06931951
Start Date
May 22 2025
End Date
December 31 2025
Last Update
October 6 2025
Active Locations (1)
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1
Daejeon Jaseng Hospital of Korean Medicine
Daejeon, South Korea