Effect of intravenous Acetaminophen for abdominal pain management in patients with acute abdome
Phase 2
Recruiting
- Conditions
- Acute abdomen.Acute abdomen
- Registration Number
- IRCT2017110427097N5
- Lead Sponsor
- Vice Chancellor for research of Ardebil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Patients above 18 years; stable vital signs; acute abdominal pain.
Exclusion criteria: Patients with a history of hypersensitivity to morphine or other opioids; proven or probable pregnancy; breastfeeding; drug addiction; get an analgesic drugs since six hours before admission to the emergency department.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain control. Timepoint: Before the intervention, 30 minuts after the intervention. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method Side Effects. Timepoint: Before the intervention, 30 minuts after the intervention. Method of measurement: Clinical examination.