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A randomized, double-blind, double-simulated, parally-controlled, multicentre trial for Zhui-Feng Tou-Gu capsule in the treatment of knee osteoarthritis

A randomized, double-blind, double-simulated, parally-controlled, multicentre trial for Zhui-Feng Tou-Gu capsule in the treatment of knee osteoarthritis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000028750
Enrollment
Unknown
Registered
2020-01-02
Start date
2019-12-31
Completion date
Unknown
Last updated
2021-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis of knee

Interventions

Sponsors

ICE of The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the American rheumatology Society (ACR) knee osteoarthritis diagnosis standard, with or without other parts of osteoarthritis; 2. It is in accordance with the diagnostic standard of cold dampness obstruction syndrome of traditional Chinese medicine; 3. Aged 18 to 70 years old; 4. Kellgren Lawrence Grade 1-3 patients; 5. VAS pain score 4 to 7; 6. Patients without surgical treatment (including arthroscopy, plastic surgery, chondrocyte transplantation, etc.); 7. Patients who did not receive intra-articular injection within 30 days; 8. Patients who have taken NSAIDs should stop using NSAIDs for at least 7 days; 9. Patients who have taken glucosamine, chondroitin sulfate and other cartilage protective drugs should stop using them for at least 30 days; 10. Voluntarily sign the informed consent form, and agree to participate in all visits, examinations and treatment in accordance with the requirements of the trial scheme.

Exclusion criteria

Exclusion criteria: 1. Patients with rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, gouty arthritis and other inflammatory arthritis; 2. Severe and unstable cardiovascular and cerebrovascular diseases (such as unstable angina, coronary vascular regeneration, cerebral vascular regeneration, transient cerebral ischemia attack, congestive heart failure, etc.), acute and uncontrollable diseases, chronic diffuse connective tissue disease, severe hypertension (blood pressure > 160 / 100mmhg) or diabetes mellitus (fasting blood glucose > 11.1mmo) not effectively controlled after treatment L/L); 3. In the past year, there were active peptic ulcer or ulcer with bleeding and perforation; 4.Patients with active liver disease or abnormal liver function (ALT or AST >=upper limit of normal value); 5. Abnormal renal function (SCR >=upper limit of normal value); 6. Those who are allergic to the test drug ingredients; 7. Pregnant, preparing pregnant or lactating women; 8. Those who are participating in other clinical trials; 9. Mental illness, no self-knowledge, unable to express or take medicine on time, unable to cooperate with the completion of the test.

Design outcomes

Primary

MeasureTime frame
Patient pain score (VAS);

Secondary

MeasureTime frame
Number of painful joints;Number of swollen joints;????????????(??VAS);WOMAC knee osteoarthritis score;TCM syndrome score;Serum ESR level of patients;Serum CRP level of patients;Serum MMP-3 level of patients;Color ultrasound of knee joint;Use of rescue drugs;

Countries

China

Contacts

Public ContactHe Yanlin

Hinye Pharmaceutical Co., Ltd

767567825@qq.com+86 15084974669

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026