Dual Endpoint Nerve Stimulation Versus Ultrasound in Infraclavicular Block for Hand Surgery

Not Applicable

Completed

• Conditions: Hand Surgery
• Interventions: Procedure: Ultrasound Guided Infraclavicular Nerve Block; Procedure: Dual-Endpoint nerve stimulation

• Registration Number: NCT00956683
• Lead Sponsor: University Health Network, Toronto

Brief Summary

Current best practice for performance of infraclavicular block dictates the use of a dual-endpoint nerve stimulation technique that still only results in a 79% success rate. Use of an ultrasound-guided technique has the potential to significantly improve success. A randomized, controlled study to evaluate this area remains to be performed and is required to demonstrate to anesthesiologists that an ultrasound-guided approach should supersede nerve stimulation as the technique of choice for infraclavicular block.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-01
• Primary Completion: 2008-08
• Study Completion: 2008-12
• Study First Submitted: 2009-07-17
• Status Verified: 2009-08
• Study First Submitted QC: 2009-08-10
• Last Update Submitted: 2009-08-10
• Study First Posted: 2009-08-11
• Last Update Posted: 2009-08-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 106

Inclusion Criteria

• Patients undergoing elective upper limb surgery at or below the elbow.
• Patients aged >18 and <80 years
• ASA I-III
• BMI<35

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Exclusion Criteria

• Inability to read, write or speak English. (This is necessary because subjects will have to follow detailed instructions to allow testing of motor and sensory function. It is not feasible to have an interpreter present in the block room during performance of these procedures)
• Contraindication to brachial plexus block
• Existing neurological deficit in the area to be blocked
• Known loco-regional malignancy or infection
• Coagulopathy
• Allergy to local anesthetic agents.
• Chest or shoulder deformities
• Severe respiratory disease
• Healed but dislocated clavicle fracture

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Ultrasound	Ultrasound Guided Infraclavicular Nerve Block	Ultrasound guided infraclavicular block
Dual Endpoint Nerve Stimulator	Dual-Endpoint nerve stimulation	Nerve stimulator guided dual endpoint infraclavicular block

Primary Outcome Measures

Name	Time	Method
To compare ultrasound-guided infraclavicular block with conventional dual-endpoint nerve stimulator guided infraclavicular block with regards to block success, ease of nerve localization, speed of onset, duration of block and complications.

Trial Locations

Locations (1)

Colin McCartney; 🇨🇦 Toronto, Ontario, Canada