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A comparative study on the effectiveness of Herbal poultice versus Diclofenac gel in relieving knee pain in osteoarthritis patients

A comparative study on the effectiveness of Herbal poultice versus Diclofenac gel in relieving knee pain in osteoarthritis patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240319008
Enrollment
60
Registered
2024-03-19
Start date
2023-03-24
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

Pain in osteoarthritis Herbal poultice, pain relief, osteoarthritis

Interventions

Study of the effectiveness of herbal poultice and diclofenac topical in reducing knee pain in patients with osteoarthritis,Study of the effectiveness of herbal poultice and diclofenac topical in reduc
Experimental Drug,Active Comparator Drug
Herbal poultice ,Diclofenac gel

Sponsors

Chulabhorn International College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Male and female, aged between 40-80 years. 2. Symptoms of osteoarthritis according to disease severity index By evaluating the Oxford Knee score, the score is in the range of 20-29 points. 3. The pain level is between 4-6 out of 10 (VAS). 4. Do not take any medicine 2 weeks before participating in the research project. 5. Can read and write Understand Thai and be able to make decisions for yourself. 6. Agree to participate in the project and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. The volunteer used other external medicines on the knee area. 2. Have you ever had an accident with your knee joint before? 3. Have ever had knee replacement surgery 4. Pain and AE have to collect and record as outcome too 5. There are plans to have surgery or transfer to another location during research participation.

Design outcomes

Primary

MeasureTime frame
Goniometer within three weeks before and after of the intervention Reported outcome using number

Secondary

MeasureTime frame
Isokinetic within twice week before and after end of the intervention Reported outcome using number

Countries

Thailand

Contacts

Public ContactNunthiya Srikaew

Chulabhorn International College of Medicine

nunthi2526@gmail.com0618243372

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026