Transient Neurologic Symptoms Clinical Trial
Official title:
Spinal Anesthesia Using Lidocaine and Sufentanil and TNS (=Transient Neurological Symptoms)
Verified date | November 2017 |
Source | Vestre Viken Ringerike Sykehus |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to find out whether patients receiving spinal anesthesia containing lidocaine and sufentanil get transient neurological symptoms.
Status | Completed |
Enrollment | 168 |
Est. completion date | May 2016 |
Est. primary completion date | May 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
Norway | Ringerike Sykehus | Hønefoss | |
Norway | Vestre Viken HF Ringerike Sykehus | Hønefoss |
Lead Sponsor | Collaborator |
---|---|
Vestre Viken Ringerike Sykehus |
Norway,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Symptoms of transient neurological symptoms | 5 days |