The Effect of Topical Sesame Oil on Severity of Pain in Patients with Limb Trauma
Phase 3
Recruiting
- Conditions
- Patients are traumatized.
- Registration Number
- IRCT20180701040297N2
- Lead Sponsor
- Research and Technology Deputy of Guilan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
the patients 18-60 years
non-penetrating trauma of the upper or lower extremities
occurrence of trauma between one to six hours prior to referral
pain score 3-6 on visual analogue scale
full consciousness
Exclusion Criteria
The presence of fractures in the injured limb
The presence of bleeding at the site of the trauma
dislocation of the injured limb
amputation of the injured limb
The presence of foreign body at the site of the trauma
The presence of neurological damage in trauma location
The presence of fever
history of sensitivity or allergy to sesame
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: The pain is totally evaluated 7 times; before the intervention on the first day and 30 minutes after each intervention for 3 days(Twice a day). Method of measurement: The Visual Analogue Scale is used to measure the severity of pain that includes a continuous line with two initial and end points of zero to 10; Zero means no pain and 10 means the maximum pain intensity.
- Secondary Outcome Measures
Name Time Method The amount of analgesic received during the intervention. Timepoint: At the end of the study. Method of measurement: Patient's document.