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Trial registered on ANZCTR
Registration number
ACTRN12608000366358
Ethics application status
Approved
Date submitted
21/07/2008
Date registered
29/07/2008
Date last updated
3/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
A comparison of arm block injection above and below the collar bone for hand surgery
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Scientific title
Speed of Onset of Ultrasound Guided Supraclavicular and Infraclavicular Brachial Plexus Block for Ambulatory Hand Surgery
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Secondary ID [1]
635
0
Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hand surgery requiring anaesthesia
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Condition category
Condition code
Anaesthesiology
3584
3584
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0
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Other anaesthesiology
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Infraclavicular block
Infraclavicular (IB) Group
The needle will be advanced just posterior to the axillary artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected.
Supraclavicular(SB) Group
The needle will be advanced superficially in a medial direction to just inferior to the brachial plexus cords just lateral to the subclavian artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected.
The duration of each procedure is approximately 15 minutes, and the overall intervention approximately 30 minutes.
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Intervention code [1]
3159
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Treatment: Devices
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Intervention code [2]
3161
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Treatment: Surgery
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Comparator / control treatment
Infraclavicular block
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Control group
Active
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Outcomes
Primary outcome [1]
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Onset time of regional arm block
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Assessment method [1]
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Timepoint [1]
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0-30 minutes, after the procedure is completed.
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Secondary outcome [1]
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Success rate for surgical anaesthesia
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Assessment method [1]
7593
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Timepoint [1]
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30 minutes, after the procedure is completed.
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Eligibility
Key inclusion criteria
Patients requiring anaesthesia for elective minor hand surgery under the care of the principal investigator
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Minimum age
No limit
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
1. Patient refusal/inability to consent
2. Allergy amide LA drugs
3. Existing neurological disorders, neuropathy of the operative extremity
4. Infection at site of needle puncture
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Subjects for the study will be recruited from/by:
1. surgeon in his rooms
2. from the operating list
3. by phone call during the week prior to surgery
4. by Participant Information Sheet mailed during the week prior to surgery
Allocation of treatment will be made by randomised number generator to assign the patient to one of the 2 groups. The allocation is concealed in sealed opaque envelopes.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated random number
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/04/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
1046
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New Zealand
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State/province [1]
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Auckland
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Funding & Sponsors
Funding source category [1]
3616
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Hospital
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Name [1]
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Anaesthesia Research Trust
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Address [1]
3616
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Park Road
Grafton
Auckland 1023
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Country [1]
3616
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New Zealand
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Primary sponsor type
Individual
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Name
Dr Michael Fredrickson
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Address
Anaesthesia Institute
P O Box 109 199
Newmarket
Auckland 1149
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
3247
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Secondary sponsor category [2]
3248
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None
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Name [2]
3248
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Address [2]
3248
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Country [2]
3248
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
5663
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Northern X Regional Ethics Committee
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Ethics committee address [1]
5663
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Private Bag 92 522 Wellesley Street Auckland
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Ethics committee country [1]
5663
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New Zealand
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Date submitted for ethics approval [1]
5663
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Approval date [1]
5663
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16/06/2008
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Ethics approval number [1]
5663
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NTX/08/04/025
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Summary
Brief summary
To determine whether ultrasound guided supraclavicular block provides more rapid onset of surgical analgesia than infraclavicular block. If the primary hypothesis is confirmed, this study will provide evidence supporting the use of the supraclavicular block for hand surgery. Increased exposure of the techniques may promote their uptake in this setting.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
28766
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Address
28766
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Country
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Phone
28766
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Fax
28766
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Email
28766
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Contact person for public queries
Name
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Dr Michael Fredrickson
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Address
11923
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Anaesthesia Institute
P O Box 109 199
Newmarket
Auckland 1149
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Country
11923
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New Zealand
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Phone
11923
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0064 9 522 1117
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Fax
11923
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0064 9 522 1127
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Email
11923
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[email protected]
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Contact person for scientific queries
Name
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Dr Michael Fredrickson
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Address
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Anaesthesia Institute
P O Box 109 199
Newmarket
Auckland 1149
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Country
2851
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New Zealand
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Phone
2851
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0064 9 522 1117
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Fax
2851
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0064 9 522 1127
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Email
2851
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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