Skip to content

Effect of Gusongling tincture combined with meloxicam tablets in the treatment of patients with knee osteoarthritis

Effect of Gusongling tincture combined with meloxicam tablets in the treatment of patients with knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100917
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Knee Osteoarthritis

Interventions

experimental group:none
control group: meloxicam

Sponsors

Mianzhu Hospital, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients who were clinically diagnosed with knee osteoarthritis met the diagnostic criteria of the Osteoarthritis Diagnosis and Treatment Guideline (2018 edition). (2) patients with mild to moderate pain symptoms requiring drug control; (3) age of 18-75 years old, both sexes; (4) no serious heart, brain, liver, kidney, lung and other important organ diseases; (5) no history of allergy to topical plaster; (6) Have not participated in other drug clinical trials in the past 6 months; (7) agree to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) severe pain requiring combination of two analgesics; (2) using analgesics within two weeks; (3) painful joint swelling or fever; (4) skin ulceration or infection at the pain site; (5) patients who were allergic to any component of the study medication and could not adhere to it; (6) patients with bone and joint dislocation, tumor, tuberculosis and other causes of neck, back and leg pain; (7) pregnant and lactating women; (8) abnormal liver and kidney function; (9) those who could not express their chief complaints correctly and could not cooperate in the study, such as patients with mental illness or severe neurosis; (10) unable to follow up regularly or cooperate with the investigators; (11) other patients considered by the investigator to be unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
knee joint function;pain;

Secondary

MeasureTime frame
Improvement of knee joint function and pain;safety evaluation;

Countries

China

Contacts

Public ContactZhang Shaojun

Mianzhu Hospital, West China Hospital, Sichuan University

zsjlovely@163.com+86 838 620 2297

Outcome results

None listed

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