Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:45 PM
Ignite Modification Date:
2025-12-24 @ 11:45 PM
NCT ID:
NCT06931951
Eligibility Criteria:
Inclusion Criteria:
* 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 Criteria:
* 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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Maximum Age:
69 Years
Study:
NCT06931951
Study Brief:
Protocol Section:
NCT06931951