KCT0009057
Not Yet Recruiting
N/A
Implementation of integrated clinical pathway in patients with non-surgical degenerative knee arthritis
Kyung Hee University Oriental Medicine Hospital at Gangdong0 sites58 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Kyung Hee University Oriental Medicine Hospital at Gangdong
- Enrollment
- 58
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Men and women over 40 years old but under 70 years old
- •2\) Those with Kellgren\-Lawrence grade 2 or 3 on knee joint radiography
- •3\) Those diagnosed with knee osteoarthritis according to the ACR (American College of Rheumatology criteria) diagnostic criteria
- •4\) Those who receive minimal help regarding their pain, are able to communicate sufficiently with the researcher, and are able to fill out the questionnaire.
- •5\) Those who voluntarily agreed to participate in this clinical trial
Exclusion Criteria
- •1\) Patients with a history of knee joint trauma or surgery on the knee joint within 6 months from the time of screening
- •2\) Patients who have received intra\-articular injection treatment within 6 months from the time of screening (steroids, hyaluronic acid, etc.)
- •3\) Patients who are suspected to have following diseases in physical examination and diagnostic examination:
- •rheumatoid arthritis, autoimmune disease, septic arthritis, inflammatory joint disease, fibromyalgia
- •4\) Patients receiving treatment for mental disorders such as depression and schizophrenia
- •5\) Patients with other diseases that may interfere with treatment, such as serious gastrointestinal or cardiovascular diseases, uncontrolled hypertension or diabetes, serious kidney or liver diseases, or hemorrhagic diseases
- •6\) Patients who have concomitant diseases which is prohibited to prescribe non\-steroidal anti\-inflammatory painkillers, hypersensitivity reactions to non\-steroidal anti\-inflammatory painkillers, and who have taken concomitant drugs.
- •7\) Pregnant and lactating women
- •8\) Participants whose participation in clinical research is determined to be difficult at the discretion of the research staff
Outcomes
Primary Outcomes
Not specified
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