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Test reliability and comparability of paper and Chinese electronic version of the Western Ontario and McMaster University osteoarthritis index

Test reliability and comparability of paper and Chinese electronic version of the Western Ontario and McMaster University osteoarthritis index

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050930
Enrollment
Unknown
Registered
2021-09-08
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

Knee osteoarthritis

Interventions

groupA:200mg celecoxib (200mg qd po)
groupB:200mg celecoxib (200mg qd po)

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients who meet the KOA diagnostic criteria of Osteoarthritis Diagnosis and Treatment Guidelines (2018 edition) issued by the Joint Surgery Group of The Orthopaedic Society of the Chinese Medical Association; 2.Aged 40 to 70 years, including 40 and 70 years, male or female. 3.KL classification <= grade 3; 4.Patients who have a mobile phone and can use the application proficiently; 5.Patients who understand Chinese language and can complete the WOMAC index independently; 6.Patients who have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with acute meniscus injury, peripheral ligament rupture injury, rheumatic arthritis, rheumatoid arthritis, peripheral tumor of knee joint, tuberculosis, idiopathic osteonecrosis of the knee; 2.Patients with serious cardiovascular, lung, liver, kidney and hematopoietic diseases, hemophilia and other hemorrhagic diseases, mental illness, pregnancy and lactation; 3.Patients who are allergic or intolerant to trial medication; 4.Patients who had received other treatments in the last 2 months has an effect on the study; 5.Patients are not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
WOMAC score;

Secondary

MeasureTime frame
WOMAC Pain subscale score;WOMAC Stiffness subscale score;WOMAC Physical Function subscale score;

Countries

China

Contacts

Public ContactYuan Wei’an
weian_1980@163.com+86 13774269261

Outcome results

None listed

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