The evaluation of Spinal Erector Plane Muscles anesthesia effect to treat post-cesarean pai

Not Applicable

Recruiting

• Conditions: Pain, Postoperative; C10.597.617

• Registration Number: RBR-5grcjzt
• Lead Sponsor: niversidade Federal de São Paulo - UNIFESP

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-09-17
• Study Completion: 2022-03-31
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Patients aged between 18 and 36 years; body mass index between 18 and 30Kg/m².

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).

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.