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Effects of Cabbage-Derived Topical Serum on Pain and Functional Outcomes in Knee Osteoarthritis: A Randomized Controlled Trial

Effects of Cabbage-Derived Topical Serum on Pain and Functional Outcomes in Knee Osteoarthritis: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260714005
Enrollment
500
Registered
2026-07-14
Start date
2023-10-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Knee Osteoarthritis Knee osteoarthritis Osteoarthritis Cabbage serum Herbal therapy Pain relief Functional outcomes Oxford Knee Score Numeric Rating Scale

Interventions

Topical application of cabbage-derived serum once daily for 12 weeks, in addition to standard care (physiotherapy and oral analgesics).,Standard care for all participants includes physiotherapy and or
Experimental Drug,Placebo Comparator Other
Cabbage serum,Placebo serum

Sponsors

Princess Srisavangavadhana Faculty of Medicine, Chulabhorn Royal Academy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Aged 50 years or older; male or female. 2. Early to moderate knee osteoarthritis, defined by clinical symptoms of knee pain and stiffness consistent with osteoarthritis, and radiographic Kellgren-Lawrence grade 2 or 3 in the target knee within the past 12 months. 3. Underwent bone mineral density (BMD) assessment via DXA scan. 4. Underwent X-rays of both hips.

Exclusion criteria

Exclusion criteria: 1. History of hip fractures or cracks on both sides. 2. Presence of conditions affecting the femur, such as metabolic bone disease, bone tumors, or bone deformity. 3. Physical condition unsuitable for undergoing X-rays and bone density testing.

Design outcomes

Primary

MeasureTime frame
Pain severity Baseline and 12 weeks post-intervention Numeric Rating Scale (NRS 0-10)

Secondary

MeasureTime frame
Knee function Baseline and 12 weeks Oxford Knee Score (OKS 0-48),Favorable clinical response rate 12 weeks Proportion achieving 3-point OKS improvement,Adverse events 12 weeks Clinical assessment and documentation,Patient satisfaction 12 weeks Satisfaction questionnaire

Countries

Thailand

Contacts

Public ContactThanapon Chobpenthai

Princess Srisavangavadhana College of Medicine, Chulabhorn Royal Academy

thanapon.cho@cra.ac.th6625766000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026