Patients with traumatic pain. Acute pain
Conditions
Interventions
The control group uses cooking oil topically
Intervention 1: The intervention group uses sesame oil extracted from tahini (Ardeh) topically. Intervention 2: The control group uses cooking oil topically.
Treatment - Other
Placebo
The intervention group uses sesame oil extracted from tahini (Ardeh) topically
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria are: age range of 15- 40 years; passing at least 1 hour and at most 6 hours from trauma; lack of any sign of bone fractures, internal or external bleeding, dislocation, amputation, presence of a foreign body, nerve damage, fever as well as infection; not using cast or splint at trauma site; having regional pain based on Visual Analog Scale (VAS); lack of any history of addiction, cigarette and alcohol abuse; not receiving drugs or herbal extracts which may interact with the study therapeutic protocol such as anti-coagulants and analgesics; and free from diseases that may a?ect the pain severity such as diabetes, cardiovascular, liver, kidney and musculoskeletal diseases.
Exclusion criteria
Exclusion criteria: Exclusion criteria are: any sign of allergy to the sesame oil or peptic or duodenal ulcers; receiving treatment out of the study like NSAIDs; inappropriate follow up by patients; and patient’s desire to withdraw in any phase of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: At first day of admission (befor intervention started) and 48 hours later. Method of measurement: Numerous ruler pain. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Gholami
Shiraz University of Medical Sciences
Outcome results
None listed