Knee Osteoarthritis Clinical Trial
Official title:
A Randomized, Double Blind, Single Simulation, Parallel Controlled, Multi-center Clinical Study of Guli Capsules in the Treatment of Knee Osteoarthritis
Previous study showed that Guli capsule could suppress the adjuvant multiple arthritis; have
inhibitory effect on carrageenan gelatinous and formaldehyde foot swelling; improve the
symptom of osteoporosis patients; and improve pain and limited joint activities of
rheumatoid patients.
To further verify the clinical effect of Guli capsule in the treatment of knee
osteoarthritis, the investigators perform this multi-center clinical study.
Status | Recruiting |
Enrollment | 220 |
Est. completion date | March 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 40 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Ages between 40 and 70 years, both gender - Kellgren and Lawrence grades of I to III; - The subjects volunteered participate in the study and complied with the regulations and signed the written consent voluntarily. - Meet the following clinical and radiological criteria for diagnosis: - Clinical criteria: 1. most of the time have knee pain nearly a month 2. bone fricative 3. morning stiffness is less than or equal to 30 min 4. age is more than or equal to 38 years 5. bony enlargement. Who meet (1) + (2) or (1) + (4) + (5) can be diagnosed as knee osteoarthritis. - Radiological criteria: 1. most of the time have knee pain nearly a month 2. the X-ray showed osteophyte formation 3. joint fluid examination confirmed with osteoarthritis 4. age is more than or equal to 40 years 5. morning stiffness is less than or equal to 30 min 6. bone fricative. Meet (1) + (2) or (1) + (3) + (5) + (6) or (1) + (4) + (5) + (6). Exclusion Criteria: - Patient with a history of allergy to similar constituents or chemical components of the drug; - Patients with limited liver and kidney function; - Patients with hematopoietic system disease; - Patients with diabetes, Cushing's syndrome and other endocrine disorders; - Patients with severe heart and brain disease; - Patients with low immunity; - Patients directly involved with the staff in the study; - Women during pregnancy or lactation; - Participating in other clinical studies or Participated in 3 months; - The investigators judged who be unfit for the study. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
China | Wangjing Hospital, Chinese Academy of Traditional Chinese Medicine | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Guizhou Bailing Group Pharmaceutical Co Ltd | People's Hospital of Guizhou Province, The First Affiliated Hospital of Guiyang College of Traditional Chinese Medicine, Wangjing Hospital, China Academy of Chinese Medical Sciences |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Osteoarthritis index on the Western Ontario and McMaster Universities Osteoarthritis Index | 4 weeks | No | |
Secondary | Pain Scores on the Visual Analog Scale | 4 weeks | No | |
Secondary | Number of Participants with Adverse Events as a Measure of Safety | 4 weeks | Yes |
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