KCT0003264
Recruiting
未知
Clinical research on the efficacy and safety of Gyebutang Granule combined with acupuncture on knee osteoarthritis
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Semyung University
- Enrollment
- 100
- Status
- Recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Adults aged 40 to 69 years.
- •2\. Those who follow the American College of Rheumatology (ACR) classification criteria for osteoarthritis of the knee and satisfy both ? and ? below.
- •? During the last 6 months, unilateral or bilateral knee arthritic pain has been reported during weight bearing activity.
- •? The knee arthritic pain is shown more than 40 ? on 100 ? Visual Analog Scale (VAS)
- •3\. Those who decide to voluntarily participate in this clinical trial and agree in signing informed consent.
- •4\. A person who is trusted and willing to cooperate with this trial for the next three months
Exclusion Criteria
- •1\. A history of knee trauma within the last 6 months.
- •2\. Operation history for the knee within the last 6 months.
- •3\. Intra\-articular injections (steroids, mucus supplements, etc.) within the last 3 months.
- •4\. The physical and diagnostic examination indicate an inflammatory arthritis such as rheumatoid arthritis, infectious disease or autoimmune disease.
- •5\. Those who are treated with mental disorders such as depression and schizophrenia.
- •6\. Patients with liver disease (AST or ALT \> normal range 2 times)
- •7\. Patients with renal disease (serum creatinine \> 2\.0 ? / ?)
- •8\. Those who have other diseases that may interfere with treatment, such as serious gastrointestinal diseases, cardiovascular diseases, hypertension, diabetes, kidney disease, liver disease, thyroid dysfunction etc.
- •9\. Those who take restrictive disease, contraindication, hypersensitivity in using the prescription of non\-steroidal anti\-inflammatory drugs (NSAIDs).
- •10\. Pregnant and lactating women.
Outcomes
Primary Outcomes
Not specified
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