Pain, Postoperative
Conditions
Interventions
Experimental group: 45 pregnant women will receive spinal anesthesia with 12mg of 0.5% hyperbaric bupivacaine, associated with the spinal erector plane block with 20 ml of 0.20% levobupivacaine on eac
Sponsors
Universidade Federal de São Paulo - UNIFESP
Universidade Federal de São Paulo - UNIFESP
Eligibility
Sex/Gender
Female
Age
18 Years to 36 Years
Inclusion criteria
Inclusion criteria: Patients aged between 18 and 36 years; body mass index between 18 and 30Kg/m².
Exclusion criteria
Exclusion criteria: Patients with skin Infection at the spinal or regional anesthesia block site; patients with cognitive impairment; patients with a history of psychiatric illness; patients using anticoagulants; patients with Diabetes Mellitus type I or II; patients with Coagulopathy; patients with history of drug abuse; patients with a history of analgesic use (up to 2 weeks before the study).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the similarity in postoperative analgesia comparing data collected using the numerical pain scale in the first 24 hours after surgery from the finding of less than 10% variation in measurements between groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find nausea and pruritus reduction in the group submitted to spinal erector plane block, verified by reduction of risk and relative risk. Data will be collected by interview 24 hours after the procedure. | — |
Countries
Brazil
Contacts
Public ContactAlan Anderson Souza
Outcome results
None listed