Pain control with intravenous Morphine versus Fentanyl in adult traumatic patients
Phase 3
- Conditions
- Adult traumatic patients.
- Registration Number
- IRCT20180608040013N1
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 180
Inclusion Criteria
Patients who have an initial pain score of 4 or more (0 = no pain and 10 = worst possible pain) according to the Numerical Rating Scale (NRS) upon presentation.
Age more than 18 years
Initial oxygen saturation greater than 95%
Patients with a GCS score of 15
Exclusion Criteria
Systolic blood pressure less than 90 mmHg
Known pregnancy
Patients with chronic pain syndromes (such as sickle cell disease or fibromyalgia)
Cognitive impairment
Known allergy to either fentanyl or morphine
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain reduction based on the Numerical Rating Scale (NRS). Timepoint: At baseline, 5, 10, 30, 120 minutes post baseline. Method of measurement: Numerical Rating Scale (NRS).
- Secondary Outcome Measures
Name Time Method Time to lowest pain score. Timepoint: From baseline to 2 hours post baseline. Method of measurement: Stopwatch.