Effects of aesthesia deep monitoring on the recovery of cesarean candidates
Not Applicable
- Conditions
- Elective cesarean.Single delivery by caesarean section
- Registration Number
- IRCT2014080218643N1
- Lead Sponsor
- Birjand University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 68
Inclusion Criteria
Natural pregnancy; 20-35 years of age; Elective cesarean; No drug use 48 hours before operation, except for iron, folic acid, and multi-vitamins; No history of diabetes, pre-eclampsia, eclampsia, hyperthyroidism, hypothyroidism, heart and renal problem, asthma, mental and psychological disorders, and addiction.
Exclusion criteria:
cesarean section duration over 45 min; Need for changes anesthesia method; Emergency situation for the mother or child; Suspect of the indicated depth according to the physician in the intervention group, and thus change in anesthesia method
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Propofol dose needed for patients. Timepoint: Drug use calculation Immediately after operation. Method of measurement: Based on received drug min/kg.
- Secondary Outcome Measures
Name Time Method Postoperative complication (nausea, vomiting, shivering, and agitation). Timepoint: During 24 hours after operation for complication. Method of measurement: Questionnaire / interview.