Spinal Anesthesia Using Lidocaine and Sufentanil and (Transient Neurological Symptoms) TNS

Vestre Viken Ringerike Sykehus168 enrolled

Overview

The purpose of this study is to find out whether patients receiving spinal anesthesia containing lidocaine and sufentanil get transient neurological symptoms.

Study Type

OBSERVATIONAL

Enrollment

168

Conditions

Transient Neurologic Symptoms

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * adults over the age of seventeen years Exclusion Criteria: * patient refuse spinal anesthesia * spinal anesthesia is contraindicated * pregnancy * patient is incapable of giving consent * diabetes * neurological disorders * chronic pain * chronic use of analgesics * spinal anesthesia within five days before the actual surgery

Locations (2)

Ringerike Sykehus

Hønefoss, Norway

Vestre Viken HF Ringerike Sykehus

Hønefoss, Norway

Outcomes

Primary Outcomes

Symptoms of transient neurological symptoms

Time frame: 5 days

Data from ClinicalTrials.gov

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