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Development and safety evaluation of "comprehensive rehabilitation instrument of traditional Chinese medicine for knee osteoarthritis"

Development and safety evaluation of "comprehensive rehabilitation instrument of traditional Chinese medicine for knee osteoarthritis" : a prospective, single-center study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071329
Enrollment
Unknown
Registered
2023-05-11
Start date
2023-05-15
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Degenerative diseases of the knee

Interventions

Manipulation group:None

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: ? In accordance with the diagnostic criteria of "knee osteoarthritis" in the Orthopaedic Society of the Chinese Medical Association (Guidelines for the Diagnosis and Treatment of Osteoarthritis) and the National Administration of Traditional Chinese Medicine (NTCM) Diagnostic Efficacy Criteria for Diseases and Syndromes of Traditional Chinese Medicine. ? age between 40 and 85 years old, including 40 and 85 years old; ? those who voluntarily participated in the observation and signed the informed consent; ? not receiving massage, physical therapy, sealing, acupuncture, small needle knife, medication and other treatments in the past 2 months.

Exclusion criteria

Exclusion criteria: ? Patients with severe cardiovascular and cerebrovascular diseases or organ failure, who could not tolerate training; ? patients with knee pain and functional limitation caused by rheumatic or rheumatoid knee arthritis, meniscus injury or dysplasia; ? Knee joint swelling and local soft tissue skin damage and red, swollen, hot, painful inflammatory reaction; ? patients with severe pain can not tolerate functional exercise; ? receiving other related treatment, which may affect the observation of effect indicators; ? patients who cannot cooperate with the study or do not agree to participate in the study or are participating in other clinical research trials

Design outcomes

Primary

MeasureTime frame
Kinematic and mechanical parameters of manipulation;

Secondary

MeasureTime frame
VAS score;KSS score;Knee range of motion;Circumference of knee joint;Knee tenderness value;

Countries

China

Contacts

Public ContactLiguo Zhu

Wangjing Hospital, China Academy of Chinese Medical Sciences

Zhlg95@aliyun.com+86 138 0103 2518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026