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The clinical effect of observation and health economics research evaluation of Subcutaneous Indwelling Needle in the treatment of mild-to-moderate knee osteoarthritis

The clinical effect of observation and health economics research evaluation of Subcutaneous Indwelling Needle in the treatment of mild-to-moderate knee osteoarthritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084517
Enrollment
Unknown
Registered
2024-05-20
Start date
2023-04-26
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Knee osteoarthritis

Interventions

treatment group:Subcutaneous Indwelling Needle

Sponsors

Shaanxi Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1)Patients who meet the diagnostic criteria for mild to moderate knee osteoarthritis; (2) Patients all between the ages of 40 and 80 years (both 40 and 80 years), both sexes; (3) Patients were enrolled unilaterally, or on the more severe side if bilateral onset; (4) No medication related to osteoarthritis of the knee within the last 1 week; (5) clear consciousness, no serious visual impairment, hearing impairment and normal cognitive comprehension; (6) Patients who voluntarily accept the content of this study and agree to sign the informed consent form. Note: Patients who must meet the above 6 criteria can be included.

Exclusion criteria

Exclusion criteria: (1) Patients who were found not to meet the inclusion criteria after enrollment; (2) Women who are pregnant or preparing to become pregnant; (3) Patients with psychiatric abnormalities and mental retardation; (4) Patients with a combination of severe cardiac, cerebrovascular, hepatic or renal pathologies or other severe metabolic abnormalities and bone tumours; (5) Patients who are also participating in other studies. Note: Patients who meet any of the above criteria should be excluded.

Design outcomes

Primary

MeasureTime frame
Knee X-ray;Western Ontario and McMaster Universities Arthritis Index;

Secondary

MeasureTime frame
visual analogue scale;knee Osteoarthritis Efficacy Evaluation Scale;

Countries

China

Contacts

Public ContactQin Weixun

Shaanxi Provincial Hospital of Chinese Medicine

qinweixun@foxmail.com+86 173 9228 5969

Outcome results

None listed

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