Effect of Ketofol and Fenofol on sedation and analgesia
Phase 2
- Conditions
- Condition 1: sedation. Condition 2: analgesia.
- Registration Number
- IRCT20160812029310N4
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 64
Inclusion Criteria
The patients at the age of 15-70 years old
ASAIII
With breast cancer
ASA I,II
candidates for lumpectomy
Exclusion Criteria
Difficult airway management
mental disorder
allergy to drugs
head Injury
Severe cardiovascular disease
Severe pulmonary disease
history of Epilepsy or Seizure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean arterial pressure. Timepoint: Before and after the intervention, one, three, five, ten minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Non invasive blood pressure Automated.;Heart rate. Timepoint: Before and after the intervention, 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Pulse oximetry device.;Arterial oxygen saturation. Timepoint: Before and after the intervention, 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes. Method of measurement: Pulse oximetry device.
- Secondary Outcome Measures
Name Time Method Intensity of pain. Timepoint: At times 1, 3, 5, 10 minutes after induction of anesthesia and then at 60 and 120 minutes after induction of anesthesia. Method of measurement: Using criterion VAS.