Complications after cesarean section. Maternal care for scar from previous cesarean delivery
Conditions
Interventions
Intervention 1: Intervention group 1: Spinal anesthesia with 2.5 cc Bupivacaine 0.5%. Intervention 2: Intervention group 2: Spinal anesthesia with 2.5 cc bupivacaine 0.5% and 10 mg tramadol. Intervent
Treatment - Other
Intervention group 1: Spinal anesthesia with 2.5 cc Bupivacaine 0.5%
Intervention group 2: Spinal anesthesia with 2.5 cc bupivacaine 0.5% and 10 mg tramadol.
Intervention group 3: Spinal anesthesia with 2.5 cc of bupivacaine 0.5% and 10-5 micrograms (equivalent to 1-2 cc) of sufentanil.
Sponsors
Semnan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: No Contraindication of Spinal Anesthesia No history of sensitivity to the three drugs used in this study and other local anesthetics no neuropathy no previous history of non-gestational cesarean Women 18 to 40 years
Exclusion criteria
Exclusion criteria: women with GI disease preterm delivery febrile women (sub-axillary temperature greater than 37.5) preeclampsia obese women (BMI> 35) cesarean delivery more than 4 times receiving antiemetic drugs 24 hours before Surgery Patients with gestational hypertension Narcotic recipients during surgery Diabetic History of PONV Receiving misoprostol Patients who cannot perform medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain relief time. Timepoint: Before and after anesthesia and after delivery (first 20 minutes, every 3 minutes and up to recovery, every 5 minutes), measurements are recorded and recorded. Method of measurement: Examination.;Chill. Timepoint: Before and after anesthesia and after delivery (first 20 minutes, every 3 minutes and up to recovery, every 5 minutes), measurements are recorded and recorded. Method of measurement: See. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham saffarieh
Semnan University of Medical Sciences
Outcome results
None listed