Comparison effect of ketamine-propofol versus fentanil-propofol forcreating analgesia and sedation during limited surgery
Phase 2
- Conditions
- Musclu-skeletal trauma.Disorder of bone density and structure, unspecified
- Registration Number
- IRCT2015082522734N2
- Lead Sponsor
- Investigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria
age between 18 to 70 y/o; Class ASA I-II
Exclusion criteria: Opium users, Sympatomimetics drug users; History of allergy and drug reaction; BMI more than 30 kg/m2
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain relief. Timepoint: 30 minute. Method of measurement: questionnare.
- Secondary Outcome Measures
Name Time Method Vital signs. Timepoint: 30 minute. Method of measurement: questionnaire.