Osteoarthritis. Polyosteoarthritis, unspecified
Conditions
Interventions
Intervention 1: The control group is prescribed a placebo for 14 days. Intervention 2: The Intervention 1 group received a topical pain reliever containing 5% frankincense per 100 grams of Oserin. Int
Sponsors
Shahid Chamran University of Ahvaz
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Osteoarthritis
Exclusion criteria
Exclusion criteria: History of joint surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score based on numerical score. Timepoint: Day 7 and day 14 after taking the medicine. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKaveh Rahimi
Shahid Chamran University of Ahvaz
Outcome results
None listed