A Randomised Comparison on the Dose Requirement Between, Levobupivacaine, Ropivacaine and Bupivacaine in Intrathecal Anaesthesia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

75 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-01-31

Study Completion Date

2008-07-31

Brief Summary

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

Detailed Description

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Conditions

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Anesthesia, Conduction Surgery

Keywords

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Patients who are going to have regional anaesthesia for lower limbs surgery. Leg Surgery.

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Combined spinal epidural anaesthesia

Intervention Type PROCEDURE

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Ying Yin Lee, Dr

Role: PRINCIPAL_INVESTIGATOR

Department of Anaesthesiology, Kwong Wah Hospital

Locations

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Kwong Wah Hospital

Hong Kong, , China

Site Status

Countries

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China

Other Identifiers

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HARECCTR0500056

Identifier Type: -

Identifier Source: secondary_id

KW/FR/05-025