The Influence of Lidocaine Volume on Discomfort During Administration of Local Anesthetic
NCT ID: NCT02086292
Last Updated: 2016-09-16
Study Results
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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COMPLETED
NA
36 participants
INTERVENTIONAL
2014-02-28
2014-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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2 milliliter lidocaine
2 ml 1% Lidocaine in one ring finger, 1 ml 2% Lidocaine in the other ring finger
2 ml 1% Lidocaine
1 milliliter lidocaine
1 ml 1% Lidocaine in one ring finger, 2 ml 2% Lidocaine in the other ring finger
1 ml 2% Lidocaine
Interventions
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2 ml 1% Lidocaine
1 ml 2% Lidocaine
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* known hypersensitivity of local anaesthetic
* renal-, heart- or liver disease
* known peripheral neuropathy or diabetes mellitus
* local infection on injection site
* circulation disorders in upper extremities (e.g. Raynaud´s phenomenon)
18 Years
65 Years
ALL
Yes
Sponsors
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St. Olavs Hospital
OTHER
Norwegian University of Science and Technology
OTHER
Responsible Party
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Principal Investigators
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Vilhjalmur Finsen, prof md
Role: STUDY_DIRECTOR
Norwegian University of Science and Technology
Locations
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Department of neuroscience, NTNU
Trondheim, , Norway
Countries
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References
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Ballo S, Hjelseng T, Tangen LF, Lundbom JS, Skarsvag T, Finsen V. The Influence of Injected Volume on Discomfort During Administration of Digital Block. J Hand Surg Asian Pac Vol. 2016 Oct;21(3):369-73. doi: 10.1142/S2424835516500363.
Other Identifiers
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2013/2297D
Identifier Type: -
Identifier Source: org_study_id
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