Elective cesarean. Single delivery by caesarean section
Conditions
Interventions
Intervention 1: Case group: The intervention group dose of anesthesia drug will be regulated in the base of BIS. Intervention 2: Control group: Controls receive the conventional anesthesia drugs.
Treatment - Drugs
Case group: The intervention group dose of anesthesia drug will be regulated in the base of BIS
Control group: Controls receive the conventional anesthesia drugs.
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Propofol dose needed for patients. Timepoint: Drug use calculation Immediately after operation. Method of measurement: Based on received drug min/kg. | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative complication (nausea, vomiting, shivering, and agitation). Timepoint: During 24 hours after operation for complication. Method of measurement: Questionnaire / interview. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRajab Arbabpour
Birjand University of Medical Sciences
Outcome results
None listed