Effect of Injection Duration on Pain and Bruising Associated with Subcutaneous Enoxapari
Not Applicable
- Conditions
- Bruising assossiated with injection.Superficial injury of unspecified body region
- Registration Number
- IRCT201110267909N1
- Lead Sponsor
- Medical University of Shahid Sadoughi Yazd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
30 – 75 years old Patients with Acute coronary syndrome; Conscious; without scar and lesion on the site of injection; Non pregnant patients; No coagulating disease
Exclusions criteria: Patient younger than 30 years old and older than 75 years old; Pregnant patients; Scar and lesion on the site of injection; Unconscious; Coagulating disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Injection site pain. Timepoint: Before injection and immediately after injection. Method of measurement: Visual Analogue Scale.;Bruising at injection site. Timepoint: 24 and 48 hours after injection. Method of measurement: per square millimeter.
- Secondary Outcome Measures
Name Time Method