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Evaluation of the clinical efficacy of Zhengqing Fengtongning sustained release tablets in the treatment of kaschin-beck disease

Evaluation of the clinical efficacy of Zhengqing Fengtongning sustained release tablets in the treatment of kaschin-beck disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076470
Enrollment
Unknown
Registered
2023-10-09
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Kaschin-Beck disease

Interventions

Zhengqing Fengtongning sustained release tablet group:Oral Zhengqing Fengtongning sustained-release tablet, 60mg/ time, twice/day, after meals, for 3 months
Etocoximab group:Oral etocoxib tablets, 30mg/ time, twice/day, after meals, for 3 months

Sponsors

The Second Affiliated Hospital of Shaanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? It meets the diagnostic criteria of KBD in Western medicine; ? It meets the standard of spleen-kidney-yang deficiency and cold-dampness-blocking collateral-type of KBD; ?Age 40-65 years old, gender is not limited; ? have been diagnosed with KBD in local medical institutions; ?Voluntarily receive randomized treatment for 3 months, and can complete the efficacy evaluation for 1 month, 3 months and 6 months of treatment; ? Volunteer to take the test and sign the informed consent.

Exclusion criteria

Exclusion criteria: ? Under 40 years old, 65 years old and above; ? Patients who received arthroscopic treatment, joint replacement and other surgical treatment during the observation period; ? Patients with cardiovascular, cerebrovascular, liver, kidney, digestive, blood system, endocrine system and other serious primary diseases and mental disorders; ? Patients with bone tumor, bone tuberculosis and non-specific inflammation; ? Lactating women and pregnant women or allergic to this medicine; ? Can not adhere to the treatment or cooperate with the efficacy of the interviewer

Design outcomes

Primary

MeasureTime frame
Visual analogue pain score;Health Status Questionnaire (SF-36 Scale);Gastrointestinal Symptom Grading Scale (GSRS);Joint dysfunction index score (according to WS/T 79-2011 "Kashin-Beck Disease Treatment Effect Evaluation");TNF-a;IL-1ß;Tinetti Balance and Gait Analysis;

Countries

China

Contacts

Public ContactKou jiushe

The Second Affiliated Hospital of Shaanxi University of Chinese Medicine

982577835@qq.com+86 138 9109 9197

Outcome results

None listed

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