Status:
TERMINATED
Comparative Study Between Bilateral and Unilateral Spinal Anaesthesia
Lead Sponsor:
University Hospital, Antwerp
Conditions:
Anesthesia; Adverse Effect, Spinal and Epidural
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
The purpose of this study is to compare unilateral spinal anesthesia using hyperbaric Prilocaine with "classical bilateral spinal anesthesia" using plain Prilocaine according to block characteristics ...
Detailed Description
Many studies have been published in search of the ideal locoregional anesthetic for day case procedures under spinal anesthesia. Transient neurological symptoms (TNS) and bladder retention are two si...
Eligibility Criteria
Inclusion
- spinal anaesthesia
- surgery\<60 minutes
Exclusion
- preexisting micturition problems
- surgery lower abdomen/pelvis
- bmi\>30
- mental problems
- kidney disease
- neurologic disease
Key Trial Info
Start Date :
December 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2014
Estimated Enrollment :
25 Patients enrolled
Trial Details
Trial ID
NCT01877356
Start Date
December 1 2012
End Date
August 1 2014
Last Update
November 14 2018
Active Locations (1)
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1
University Hospital Antwerp
Edegem, Antwerp, Belgium, 2650