Evaluation of preventive effect of injection paracetamol and lidocaine in reducing pain caused by intravenous injection of propofol in childre
Phase 3
Recruiting
- Conditions
- Inguinal herniaInguinal surgery.
- Registration Number
- IRCT20200825048515N34
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Children 4-6 years
Has the American Association of Anesthesiologists (ASA) One and Two
Candidate for inguinal surgery under general anesthesia with propofol
Exclusion Criteria
Has underlying diseases (including liver, cardiovascular, neurological, metabolic disease, dermatitis)
Having drug allergies
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score. Timepoint: During injection of propofol. Method of measurement: Behavioral scale derived from the Face, Leg, Activity, Cry, Consolability (FLACC).;Agitation score. Timepoint: During injection of propofol. Method of measurement: According to Richmond criteria.;Mean Arterial Pressure. Timepoint: Before and one minute after the intervention. Method of measurement: Monitoring device.;Hear rate. Timepoint: Before and one minute after the intervention. Method of measurement: Monitoring device.
- Secondary Outcome Measures
Name Time Method