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NCT Number: NCT01283087
Spinal Anesthesia Using Lidocaine and Sufentanil and (Transient Neurological Symptoms) TNS
The purpose of this study is to find out whether patients receiving spinal anesthesia containing lidocaine and sufentanil get transient neurological symptoms.
Completed
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Ringerike Sykehus, Hønefoss, Norway
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Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Primary outcomes
-
Symptoms of transient neurological symptoms
Time frame: 5 days
Sponsors and collaborators
Lead sponsor
Vestre Viken Ringerike Sykehus
Other
Registry information
Official study title
Spinal Anesthesia Using Lidocaine and Sufentanil and TNS (=Transient Neurological Symptoms)
Important dates
- Study start
- 2011
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Jan 25, 2011
- Registry last updated
- Nov 27, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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