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Efficacy and Mechanism of Huangdi Internal Acupuncture versus Non-Steroidal Anti-Inflammatory Drug (Celecoxib) for Moderate Knee Osteoarthritis: A Randomized, Assessor-Blinded, Controlled Trial

Efficacy and Mechanism of Huangdi Internal Acupuncture versus Non-Steroidal Anti-Inflammatory Drug (Celecoxib) for Moderate Knee Osteoarthritis: A Randomized, Assessor-Blinded, Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000999
Enrollment
Unknown
Registered
2026-04-16
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Moderate Knee Osteoarthritis

Interventions

Huangdi Internal Acupuncture Group:Huangdi Internal Acupuncture
Celecoxib Group:Celecoxib Capsules

Sponsors

Yantai Yuhuangding Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 45–75 years. 2. Meet clinical diagnostic criteria for knee osteoarthritis with Kellgren-Lawrence grade II or III. 3. Average resting pain VAS score =4 (0–10 scale) in the target knee during the past week before screening. 4. For bilateral KOA, the more painful knee is designated as the target knee. 5. Voluntarily participate and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Received intra-articular injections (corticosteroids, hyaluronic acid, platelet-rich plasma, etc.) in the target knee within the past 3 months. 2. History of knee surgery (including arthroscopy) on the target knee, or planned knee surgery within the next 6 months. 3. Secondary arthritis (e.g., rheumatoid arthritis, ankylosing spondylitis, acute gouty arthritis, infectious arthritis, etc.). 4. Severe cardiovascular, cerebrovascular, hepatic, or renal insufficiency, coagulation disorders, or psychiatric disorders. 5. Known allergy or contraindication to celecoxib (e.g., sulfonamide allergy) or to diclofenac sodium. 6. Pregnant, planning pregnancy, or breastfeeding. 7. Currently participating in another interventional clinical trial. 8. Have used any of the following drugs within the first 4 weeks of enrollment: long-acting opioid analgesics (such as morphine, hydrocodone, fentanyl, etc.), antidepressants (such as amitriptyline, duloxetine, etc.), anticonvulsants (such as gabapentin, pregabalin, etc.), or other central nervous system drugs that may significantly affect pain perception (as determined by the researcher); The use of acetaminophen (daily dose = 2g) as a temporary remedial medication is allowed, but it needs to be recorded.

Design outcomes

Primary

MeasureTime frame
Pain intensity;Joint function and symptoms;

Secondary

MeasureTime frame
Synovial inflammation of knee joint (ultrasound);Specific knee joint function;Quality of life;Patient's overall improvement impression;Use of corrective medications;

Countries

China

Contacts

Public ContactZhang Jing

Yantai Yuhuangding Hospital

738866564@qq.com15966463183

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026