cesarean. Delivery by elective caesarean section
Conditions
Interventions
Intervention 1: Group1 : bupivacaine 0.5% (8mg), 15 micrograms fentanyl and 0.1 ml normal saline total volume 2ml. Intervention 2: Group2 :intrathecal bupivacaine 0.5% (8mg), 15 mg of meperidine and 0
Treatment - Drugs
Group1 : bupivacaine 0.5% (8mg), 15 micrograms fentanyl and 0.1 ml normal saline total volume 2ml.
Group2 :intrathecal bupivacaine 0.5% (8mg), 15 mg of meperidine and 0.1 ml normal saline total volume 2ml.
Group3:intrathecal bupivacaine 0.5% (10 mg) (total volume 2 ml)
Sponsors
Vice Chancellor for Research; Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: pregnant women, ASA I-II with singleton pregnancies who were underwent elective Caesarean section, Exclusion criteria: Patients with cardiovascular disorders, renal failure, coagulopathy, sensitivity to the drugs, preeclampsia, lack of consent and spinal anesthesia contraindication, history of seizures or other neurological diseases, (IUGR).
Exclusion criteria
Exclusion criteria:
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| To determine the duration of sensory block in patients receiving intrathecal meperidine with bupivacaine 0.5%. Timepoint: Prioperative and post operative. Method of measurement: Pinprick Scale. | — |
Primary
| Measure | Time frame |
|---|---|
| Determine the duration of sensory block in patients with intrathecal fentanyl added to bupivacaine 0.5%. Timepoint: Perioperative and Post-operative. Method of measurement: Pinprick. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAzadeh Azizolahi
Shiraz University of Medical Sciences
Outcome results
None listed