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The effect of topical use of sesame oil extracted from tahini (Ardeh) on pai

Not Applicable
Conditions
Patients with traumatic pain.
Acute pain
Registration Number
IRCT20171017036838N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
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 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.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: At first day of admission (befor intervention started) and 48 hours later. Method of measurement: Numerous ruler pain.
Secondary Outcome Measures
NameTimeMethod
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