Sedative and anesthetic effect of hypnotism versus propofol and dexmedetomidine and component of midazolam-fentanyl in aware and awake patient in ICU ward
Phase 2
- Conditions
- Head injury.Superficial injury of head
- Registration Number
- IRCT201608189014N110
- Lead Sponsor
- Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
age of 18 to 50 years; literate at least diploma; need mechanical ventilation with any reason.
Exclusion criteria: consciousness disorder; acid-base disorder; psychiatric disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing agitation. Timepoint: before intervention and 20, 40, 60 min and 1, 2, 6, 12, and 24 hours after intervention. Method of measurement: through physical examination.;Assessing pain. Timepoint: before intervention and 20, 40, 60 min and 1, 2, 6, 12, and 24 hours after intervention. Method of measurement: using VAS scale.
- Secondary Outcome Measures
Name Time Method Assessing adverse effect (hypotension, apnea, bradycardia). Timepoint: 20, 40, 60 min and 1, 2, 6, 12, and 24 hours after intervention. Method of measurement: through physical examination.