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

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01283087

Enrollment

168

Registered

2011-01-25

Start date

2011-01-31

Completion date

2016-05-31

Last updated

2017-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transient Neurologic Symptoms

Keywords

TNS, Spinal anesthesia, Lidocaine

Brief summary

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

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame
Symptoms of transient neurological symptoms	5 days

Countries

Norway

Outcome results