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

Vestre Viken Ringerike Sykehus

Status: Completed

Conditions: Transient Neurologic Symptoms

Study type: Observational

Funder types: Other

Identifiers

NCT01283087

400229

Details and patient eligibility

About

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

Enrollment: 168 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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