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Clinical Study on the Treatment of Knee Osteoarthritis with the Deep Healing Light Moxibustion Device Based on Micro-Nano Optical Bio-Intervention Technology

Clinical Study on the Treatment of Knee Osteoarthritis with the Deep Healing Light Moxibustion Device Based on Micro-Nano Optical Bio-Intervention Technology

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125693
Enrollment
Unknown
Registered
2026-05-29
Start date
2024-12-05
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Knee Osteoarthritis

Interventions

Single group (self-controlled before-after study), without parallel control group.:Use the Deep Spasm Light Moxibustion Device for red light irradiation therapy. The specific procedure: fix the light

Sponsors

The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for knee osteoarthritis according to the Guidelines for the Diagnosis and Treatment of Osteoarthritis (2018 Edition), sign the informed consent form, and be willing to actively cooperate with treatment observation; 2. Have not taken other medications or received other treatments (e.g., surgery) within the past 4 weeks; 3. Aged 50 to 80 years (inclusive), both genders; 4. Kellgren-Lawrence (K-L) grade on X-ray is Grade II or below (including Grade II); 5. Have a follow-up period of at least 4 weeks.

Exclusion criteria

Exclusion criteria: 1. Those who do not receive treatment as prescribed or have incomplete clinical data; 2. Those who are unwilling to cooperate with clinical treatment observation; 3. Patients with gout, rheumatism, or rheumatoid arthritis; 4. Patients with serious underlying diseases such as cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, and/or hematopoietic system disorders, or those with mental illness; 5. Patients with severe developmental deformities of the knee joint; 6. Patients with osteoarthritis caused by osteomyelitis, bone tumors, or bone tuberculosis, or those with traumatic arthritis caused by trauma.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) for pain;Hospital for Special Surgery (HSS) Knee Score;Lysholm Knee Scoring Scale;

Countries

China

Contacts

Public ContactYao Jinghui

The Third Affiliated Hospital of Southern Medical University

yaojinghui@smu.edu.cn+86 137 2486 9010

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026