Different Anesthesia Methods on Development of Postnatal Depression After Cesarean Delivery
Pregnancy Related
About this trial
This is an interventional treatment trial for Pregnancy Related focused on measuring Anesthesia, Postnatal depression, Cesarean delivery
Eligibility Criteria
Inclusion Criteria:
- Aged 21-50 years old
- 36 gestational weeks or more,
- American Society of Anesthesiologists' (ASA) I and II
- Able to communicate
Exclusion Criteria:
- history of bipolar or psychotic disorder
- suicidal state
- Chronic pain syndrome
- Intraoperative complication
- drug and/or alcohol abuse
- who did not want to participate
- emergency cases
- unable to communicate in Turkish
Sites / Locations
- Istanbul Medipol University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Grup I= General anesthesia group
Grup II= Spinal anesthesia group
After applying standard ASA monitoring; 2-2,5 mg/kg propofol, and 0,6 mg/kg rocuronium IV will be performed for general anesthesia induction, and then orotracheal intubation will be performed. The patients will be placed in the supine position. General anesthesia will be maintained with sevoflurane in the mixture of oxygen-fresh air. Controlled mechanical ventilation will be initiated with a tidal volume of 8-10 ml/kg at 12 breaths per minute (I:E ratio 1:2), a fresh gas flow rate of 2 L per min, end tidal CO2 value at 30-35 mmHg, and peak airway pressure of maximally 30 cm H2O. All patients will undergo cesarean delivery surgery with the same technique by the same surgical team.
A standardized spinal anesthesia will administrated to the patients. After skin disinfection, 25G needle will used for puncture at the level of L2-L3 or L3-L4. After observing the cerebrospinal fluid, 15 mg bupivacaine (marcain spinal heavy) will be administered into the subarachnoid space. The level of anesthesia below T6 will be controlled.