Effect of time and place of subcutaneous injection of Enoxaparin on the severity of pain and size of bruising
Not Applicable
Recruiting
- Conditions
- Pain and bruise.
- Registration Number
- IRCT20150106020581N2
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Age range 20 to 75 years
Physiological stable condition
Being able to understand and express pain
Platelet count in normal range
Body mass index (BMI) ranging from 18.5 to 30
Exclusion Criteria
Analgesic use, four hours before the intervention
Swelling, ulcer, scratches and erythema in the injection site
Muscular and dermal disease and Known coagulopathy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: Immediately after subcutaneous injection of Enoxaparin. Method of measurement: Visual-Analogue Scale of pain(VAS).;Bruising size. Timepoint: 24 and 48 hours after each subcutaneous injection of Enoxaparin. Method of measurement: Transparent millimeter ruler.
- Secondary Outcome Measures
Name Time Method