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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00636974
Other study ID # KW/FR/05-025
Secondary ID HARECCTR0500056
Status Completed
Phase N/A
First received December 19, 2007
Last updated October 22, 2013
Start date January 2006
Est. completion date July 2008

Study information

Verified date October 2013
Source Hospital Authority, Hong Kong
Contact n/a
Is FDA regulated No
Health authority Hong Kong: Ethics Committee
Study type Interventional

Clinical Trial Summary

To determine and compare the effective intrathecal dose of levobupivacaine, ropivacaine and bupivacaine for 50% of patients in lower limb surgery


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date July 2008
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- body weight=40-90kg,

- height higher than 145cm

Exclusion Criteria:

- Known hypersensitivity to amide local anaesthetics,

- patients who do not understand English and Chinese,

- Body mass index higher than 35 kg per sq metre

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Combined spinal epidural anaesthesia


Locations

Country Name City State
China Kwong Wah Hospital Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Hospital Authority, Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensory block at 12th thoracic dermatome or above and successful conduct of the lower limb surgery up to 50 minutes after the intrathecal injection of the study drug 50 minutes after the intrathecal injection of the study drug
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