se of Topical Anesthetic Cream for pain relief caused by the injection of Spinal Anesthesia in elective cesarean sections

Not Applicable

• Conditions: Complications of anesthesia given during pregnancy; Contact with hypodermic needle

• Registration Number: RBR-29xb94
• Lead Sponsor: Financiamento Próprio

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-03-15
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Female patients; over 18 years; pregnant women (above 37 weeks); physical status ASA II; to be submitted to subarachnoid anesthesia for elective cesarean surgery.

Exclusion Criteria

Will not be included in the study: Patients who refuse to participate in the study; patients in labor; who are taking any sedative, opioid or sleep inducing drugs; who have a history of allergy to any drug to be used in the study; severe obesity (defined by a BMI of more than 35 kg.m2), methemoglobinemia, carriers of pathologies that cause some cognitive deficit, such as schizophrenia, oligophrenia, severe depression, etc. If this occurs, the patients will be excluded from the clinical trial, but will not suffer harm in their treatment.
Patients who begin labor during the latency period of topical medication, who require cesarean section before completing 60 minutes after application of the patch containing the cream (anesthetic or placebo), who request their exclusion from the study, will be excluded from the study. study during their performance, who present an allergic reaction during anesthesia or who present partial or total failure of the anesthetic block.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
evel of pain during local anesthesia with lidocaine measured by visual analogue pain scale

Secondary Outcome Measures

Name	Time	Method
Pain assessment reported by the patients through visual analog pain scale after lumbar puncture.;Check if patients prefer to receive the dermatological anesthetic cream used in a next anesthesia.