A comparative trial on hemodynamic changes caused by anesthesia with propofol-remifentanil and isoflurane-remifentanil
Phase 3
Recruiting
- Conditions
- Anesthesia in cleft palate.
- Registration Number
- IRCT20180520039739N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Age < 3 years old
American Society of Anesthesiologists (ASA) Class I
Exclusion Criteria
Congenital cardiac or pulmonary diseases
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure. Timepoint: q 15 min. Method of measurement: Manometer.;Heart rate. Timepoint: q 15 min. Method of measurement: Heart monitoring.
- Secondary Outcome Measures
Name Time Method