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Clinical Trials/NCT01283087
NCT01283087
Completed
Not Applicable

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

Vestre Viken Ringerike Sykehus2 sites in 1 country168 target enrollmentJanuary 2011
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ConditionsTransient Neurologic Symptoms

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Transient Neurologic Symptoms
Sponsor
Vestre Viken Ringerike Sykehus
Enrollment
168
Locations
2
Primary Endpoint
Symptoms of transient neurological symptoms
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
May 2016
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Vestre Viken Ringerike Sykehus
Responsible Party
Principal Investigator
Principal Investigator

Britt-Marie Berling

MD, PhD

Vestre Viken Ringerike Sykehus

Eligibility Criteria

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
  • •neurological disorders
  • •chronic pain
  • •chronic use of analgesics
  • •spinal anesthesia within five days before the actual surgery

Outcomes

Primary Outcomes

Symptoms of transient neurological symptoms

Time Frame: 5 days

Study Sites (2)

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