Knee Osteoarthritis
Conditions
Brief summary
This study evaluates the efficacy and safety of Panlongqi tablet compared with placebo in the treatment of knee osteoarthritis in adults.Half of participants will receive Panlongqi tablet in combination,while the other half will receive a Placebo.
Detailed description
The test group will be given Panlongqi tablet 1.2g three times per day,the control group will be given placebo 1.2g three times per day. The invention will last 4 weeks.
Interventions
DRUGTreatment of Panlongqi Tablet
Panlongqi Tablet:1.2g,3times a day, oral, for 4 weeks.
DRUGTreatment of Panlongqi placebo
Panlongqi placebo:1.2g,3times a day, oral, for 4 weeks.
Sponsors
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1.40-75 years of age (including 40 years and 75 years old), men and women are not limited. 2\. western medicine diagnosis of knee osteoarthritis, clinical classification for primary. 3.The severity of the imaging classification of K-L≤Ⅲ; 4. treatment VAS pain scores than 40mm (select the subjects most obvious limb pain symptoms). 5\. informed consent form signed by the patient or legal representative.
Exclusion criteria
1. within 3 months prior to the trial, the patients were treated within 1 years. 2. 4 weeks before the treatment, corticosteroids, non steroidal drugs, intra-articular injections or other drugs to improve the condition (such as cartilage protective agents) were used. 3. Swelling of the knee joint. 4. knee synovial crystalline (joint) inflammation, acute inflammatory arthritis, rheumatoid arthritis, metabolic bone disease, psoriatic arthritis, septic arthritis, systemic lupus erythematosus, Sjogren syndrome, vasculitis and other rheumatic diseases caused by inflammatory arthritis and endocrine diseases caused by. 5. the screening period has any disease history or evidence: The basic of serious cardiovascular and cerebrovascular diseases; An active, recurrent peptic ulcer or other hemorrhagic disease risk; Sales and other serious diseases of digestive system; An associated with malignant tumors, blood, or other serious diseases or system; 6. patients who are unable to cooperate or cooperate with other mental disorders. 7. before the screening, any laboratory test indicators meet the following standards: An admission of liver and kidney function showed that ALT and AST is more than 1.5 times the upper limit of the normal value, Cr is more than 1.2 times the upper limit of normal (Reference Research Center laboratory where the range of normal value); An other clinically significant laboratory abnormalities, and the researchers judged not into the group. 8. allergic constitution or allergic to test seven tablets, excipients or similar ingredients; 9. doubt or indeed history of alcohol and drug abuse; 10. pregnant or lactating women or recent planned pregnancies and those who are reluctant to use contraceptives; 11. participants who participated in other clinical trials within the first 3 months. 12. the researchers believe that patients should not participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The change from Baseline to week 4 in Visual Analog Scale (VAS)score | 0 weeks,2 weeks，4 weeks | VAS scores ranges from 0 to 100, with higher scores indicating heavier pain |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The change from Baseline to week 4 in Western Ontarioand McMaster Universities Osteoarthritis Index (WOMAC)score | 0 weeks,2 weeks and 4 weeks | WOMAC scores ranges from 0 to 96, with higher scores indicating greater disability |
| The change from baseline to week 4 in The Short Form-36 Health Survey (SF-36) scores | 0 weeks,4 weeks | SF-36 scores ranges from 0 to 100,it shows the extent of physical function restriction with higher scores indicating greater disability |
| The number of adverse events | 4 weeks | The number of adverse events related to treatment. |
Countries
China
Contacts
Primary ContactJiang Quan, Doctor
Outcome results
None listed