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Observation of cartilage ultrastructure, gait and therapeutic effect of needle-knife based on "tendon-regulating and bone-setting" on KOA patients

Observation of cartilage ultrastructure, gait and therapeutic effect of needle-knife based on "tendon-regulating and bone-setting" on KOA patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091207
Enrollment
Unknown
Registered
2024-10-23
Start date
2024-10-31
Completion date
Unknown
Last updated
2024-10-28

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:Needle-knife treatment using the "tendon-regulating and bone-setting", with needle-knife treatment points selected at the anterior, lateral, posterior and medial sides of the knee join
Control group:Oral celecoxib capsules (Celebrex, Pfizer Pharmaceuticals, NDT: J20140072,200 mg), 200 mg once daily for 3 weeks.

Sponsors

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: a. Meet the diagnostic criteria of the Chinese Osteoarthritis Diagnosis and Treatment Guidelines (2021 edition) issued by the Chinese Medical Association. b. No other systemic diseases; c. No medication or other treatment in the last 2 weeks; d. Sign the informed consent form and participate in the experiment regularly according to the requirements of the experiment.

Exclusion criteria

Exclusion criteria: a. Unable to cooperate or unsuitable for needle knife treatment; b. Allergy to sulfonamides; c. Patients with heart, liver, kidney and other primary diseases or mental diseases; d. Patients with other knee joint diseases (such as infection, tuberculosis, rheumatoid, trauma, skin disease, etc.); e. Pregnant and breast-feeding females; f. Patients with critical conditions who are difficult to independently evaluate the efficacy and safety of the treatment; g. Those who have difficulty in adhering to the established program of treatment and affecting the progress of the subject.

Design outcomes

Primary

MeasureTime frame
T2*mapping analysis;Gait analysis;Visual Analogue Scale (VAS);Knee score (HSS);

Countries

China

Contacts

Public ContactZheng Zhiweng

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine

924596673@qq.com+86 137 3922 1736

Outcome results

None listed

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