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)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

University Hospital Antwerp

Edegem, Antwerp, Belgium, 2650