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A study on pain relieving property of a herbal lotion for joint pains

Evaluation of the efficacy of Orthosheild lotion for joint pains: An open-label clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN29999260
Enrollment
70
Registered
2026-01-06
Start date
2025-12-15
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Joint pain and musculoskeletal discomfort Musculoskeletal Diseases

Interventions

This is a single-arm open-label clinical trial conducted among patients diagnosed with mild to moderate joint pain. Eligible participants will apply Ortho Shield Herbal Lotion twice daily (morning and

Sponsors

Fadna Life Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Adults aged 20–70 years, of either sex. 2. Diagnosed with mild to moderate arthritis or musculoskeletal pain for more than two weeks. 3. Willing to provide written informed consent. 4. Able to comply with the study protocol and follow-up schedule.

Exclusion criteria

Exclusion criteria: 1. Patients with serious systemic illnesses (e.g., rheumatoid arthritis, lupus, HIV). 2. Pregnant or breastfeeding women. 3. Patients currently using other pain-relieving topical or systemic medications. 4. Known hypersensitivity or allergy to any component of the lotion. 5. Presence of open wounds or infections at the application site.

Design outcomes

Primary

MeasureTime frame
1.Reduction in joint pain intensity measured using the McGill Pain Questionnaire at baseline and after two weeks of intervention. 2.Improvement in overall quality of life scores (QOL) assessed before and after treatment.

Secondary

MeasureTime frame
1. Assessment of skin sensitivity and local adverse reactions (e.g., redness, itching, swelling). 2. Change in blood pressure and heart rate before and after the intervention. 3. Participant-reported satisfaction and functional improvement scores.

Countries

Sri Lanka

Contacts

Public ContactPathirage Kamal Perera
kamalperera@fim.cmb.ac.lk+94 716419072

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 21, 2026