Pain after cesarean section. Delivery
Conditions
Interventions
Intervention 1: Intervention group 1: 10 mg of 0.5% bupivacaine with 25 micrograms of fentanyl prescribed intrathecally into cerebrospinal fluid, at the space between the vertebrae 4 and 5 lumbar in t
Treatment - Drugs
Intervention group 1: 10 mg of 0.5% bupivacaine with 25 micrograms of fentanyl prescribed intrathecally into cerebrospinal fluid, at the space between the vertebrae 4 and 5 lumbar in the midline, usin
Intervention group 2: 10 mg of 0.5% bupivacaine with 25 micrograms of sufentanil prescribed intrathecally into cerebrospinal fluid, at the space between the vertebrae 4 and 5 lumbar in the midline, us
Sponsors
Vice Chancellor for research of Hormozgan University of Medical Sciences, Bandar Abbas.
Eligibility
Sex/Gender
Female
Age
10 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: class ? or ? of ASA (American Society of Anesthesiologists; candidate for elective cesarean section; no history of heart disease, hypertension, preeclampsia, gestational diabetes; being satisfied to receive intrathecal anesthesia and participate in the study. Exclusion criteria: contraindication for spinal anesthesia; presence of infection in the needle insertion site; high intracranial pressure; coagulopathy; platelet count lower than 75000.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The numbness. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire.;Blood Pressure. Timepoint: Monitoring during the first 24 hours. Method of measurement: Questionnaire.;Analgesia. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea and vomiting. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAbbas Pak Nahad
Anaesthesiology, Critical Care and Pain Management Research Center, Hormozgan University of Medical
Outcome results
None listed