Status:
COMPLETED
A Randomised Comparison on the Dose Requirement Between, Levobupivacaine, Ropivacaine and Bupivacaine in Intrathecal Anaesthesia
Lead Sponsor:
Hospital Authority, Hong Kong
Conditions:
Anesthesia, Conduction
Surgery
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
To determine and compare the effective intrathecal dose of levobupivacaine, ropivacaine and bupivacaine for 50% of patients in lower limb surgery
Eligibility Criteria
Inclusion
- body weight=40-90kg,
- height higher than 145cm
Exclusion
- Known hypersensitivity to amide local anaesthetics,
- patients who do not understand English and Chinese,
- Body mass index higher than 35 kg per sq metre
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2008
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT00636974
Start Date
January 1 2006
End Date
July 1 2008
Last Update
October 23 2013
Active Locations (1)
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1
Kwong Wah Hospital
Hong Kong, China