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A randomized controlled trial for comparing the effect of moxibustion by using different moxas from different habitats in the treatment of moderate and severe primary knee osteoarthritis

Effect assessment of moxibustion with moxa from different habitats for moderate and severe primary knee osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008031
Enrollment
Unknown
Registered
2016-02-23
Start date
2016-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

knee osteoarthritis

Interventions

moxa 1 group:moxibustion with moxa from Qichun, Hubei province
moxa 2 group:moxibustion with moxa from Nanyang, Henan province
non-moxa group:moxibustion with Herba Artemisiae Capillariae

Sponsors

Acupuncture and moxibustion hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged 50 to 80 years; (2) Meeting the diagnostic criteria of primary knee osteoarthritis; (3) The Womac osteoarthritis index scores at total of 48 to 72, rated as a moderate to severe disease grade, after the stop of drugs for knee osteoarthritis (including non-steroidal anti-inflammatory drugs, analgesic, Chinese herbs or Chinese patent medicine) for 3 days; (4) The Kellgren and Lawrence grades of knee osteoarthritis is grade 2 or grade 3.

Exclusion criteria

Exclusion criteria: (1) Secondary knee osteoarthritis; (2) The target knee joint had a history of trauma or surgery in the recent year , or had severe deformity; (3) The target knee joint was received intra-articular injection of corticosteroid in the past three months, or received intra-articular injection of sodium hyaluronate, acupuncture or moxibustion in the past two weeks; (4) Symptomatic hip osteoarthritis or patella osteoarthritis in the same side as the target knee joint; (5) Inflammatory or other rheumatic disease; (6) Acute meniscus injury of knee joint, or acute ligamentous injury or rupture of knee joint; (7) Tumor, tuberculosis or spontaneous osteonecrosis of knee joint; (8) Patients who have to take paracetamol, non-steroidal anti-inflammatory drug or analgesic for the control of other diseases; (9) Uncontrolled hypertension or diabetes, or serious cardiovascular, cerebral, lung, liver, kidney, or hematopoietic system disease, malignant tumor, hemorrhagic disease, or psychiatric disease; (10) Scar diathesis or cutaneous sensory disorder; (11) Pregnant or lactating women; (12) Patients who refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
WOMAC pain score;VAS score of knee pain;

Secondary

MeasureTime frame
The total score, stiffness subscale score and physical function subscale score of WOMAC;proportion of patients acheiving clinical improvement;general assessment of patients;amount of articular effusion in knee joint;

Countries

China

Contacts

Public ContactHong Zhao
hongzhao2005@aliyun.com+86 13911132103

Outcome results

None listed

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