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Clinical case control study of the clinical phenomenon and regularity of acupoint sensitization of Knee Osteoarthritis in China

Clinical case control study of the clinical phenomenon and regularity of acupoint sensitization of Knee Osteoarthritis in China

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014732
Enrollment
Unknown
Registered
2018-01-31
Start date
2016-10-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

Knee osteoarthritis

Interventions

Sponsors

Chengdu university of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. diagnosed as KOA according to the guidelines for the diagnosis and treatment of knee osteoarthritis in adults CG177; 2. aged from 40 to 80 years old; 3. Good compliance and agree to be examined provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. merged with other diseases but not belong to osteoarthritis, such as tuberculosis, cancer of bones and joints, and rheumatism and rheumatoid arthritis; 2. merged sprain or by traumatic injury; 3. talipes and pain with foot and other diseases affecting normal walking; 4. serious diseases including angiocardiopathy, impaired renal and liver function, autoimmune disease, diabetes and blood disease; 5. having received the traumatic therapy due to KOA within the previous 1 months.

Design outcomes

Primary

MeasureTime frame
the examination of morphological changes;the detection of sensory of body’s surface;physical characteristics test of acupuncture points;

Secondary

MeasureTime frame
Western Ontario and McMaster University Osteoarthritis Index ;simplified McGill pain questionnaire;Quality of life scale SF-12;

Countries

China

Contacts

Public ContactFanron Liang

Chengdu university of Traditional Chinese Medicine

arcuresearch@126.com+86 028-69950657

Outcome results

None listed

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