Clinical trial comparing effect of Paracetamol and Ketorolac on pain management after cardiac surgery in childre
Phase 3
- Conditions
- Precordial pain.Precordial pain
- Registration Number
- IRCT2015012320759N1
- Lead Sponsor
- Vice Chancellor for Research, Mashhad University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
All patients undergoing cardiac surgery; children between the age of 12-2 years. Exclusion criteria: patient dissatisfaction; addiction; drug allergy. Ketorolac groups: patients with renal insufficiency. Parecetamol group having allergies; liver failure; renal failure
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Every 1 hour to 24 hours after the second day every 4 hours for 48 hours. Method of measurement: CPOT (Critical-care Pain Observation Tool).
- Secondary Outcome Measures
Name Time Method