Comparison of the effect of ketorolac, morphine, and apotel in patients with head trauma
Phase 2
- Conditions
- Head trauma.Other and unspecified injuries of head
- Registration Number
- IRCT201603089014N94
- Lead Sponsor
- Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 105
Inclusion Criteria
age of 15 to 50 years;
head trauma during 24 hours
severity of headache equal to or greater than 4 based on VAS
Exclusion Criteria
Decreased consciousness
Abnormal neurologic findings
Hemorrhagic and pathologic findings in brain CT scan
A history of hemorrhagic disorders or using anti-coagulant agents
A history of chronic headaches
Multiple trauma
Asthma
Addiction
Pregnancy
Renal failure, liver disease, cardiovascular diseases, pulmonary diseases
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measuring the severity of headache. Timepoint: before, and 15 and 30 min after intervention. Method of measurement: using visual analog scale (VAS).
- Secondary Outcome Measures
Name Time Method Assessing probable drug side effects (such as nausea, vomiting, dizziness, itching). Timepoint: 15 and 30 min after intervention. Method of measurement: by question.