Cesarean section. Delivery by caesarean section, unspecified
Conditions
Interventions
Intervention 1: Intervention group: All patients will undergo spinal block. After performing the spinal block and confirming its accuracy, patients will be prescribed a combination of 0.5 mg of neosti
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Pregnant woman candidate for cesarean section with spinal anesthesia American anesthesiologists association classification I and II Age 18-45 years No neurological deficit in limb, spinal cord and CNS No coagulation diseases No history of spinal cord surgery, spinal canal stenosis and MS Duration of surgery less than 2 hours No heart conductive disorder No history of migraine headaches No anticoagulant drug consumption Consent for spinal block Patient consent to participate in the study
Exclusion criteria
Exclusion criteria: Spinal block failure Change in anesthesia method to general anesthesia Bleeding more than 20 cc/kg More than 3 punctures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache severity. Timepoint: From first day to five days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Duration of headache. Timepoint: From first day to five days after surgery. Method of measurement: Counting the number of days suffering from headache. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLili Adineh Mehr
Esfahan University of Medical Sciences
Outcome results
None listed