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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00321425
Other study ID # S-05240
Secondary ID
Status Completed
Phase N/A
First received May 2, 2006
Last updated May 20, 2008
Start date May 2006

Study information

Verified date October 2007
Source Rikshospitalet University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

In an observer-blinded study ultrasound guidance and electrical nerve stimulation will be compared for lateral sagital infraclavicular blocks (LSIB). Block effectiveness, time consumption and patient acceptance will be registered in 80 patients. Ultrasound guidance may cause less discomfort and could be less time consuming than electrical nerve stimulation.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Infraclavicular brachial plexus block

- Hand surgery

Exclusion Criteria:

- ASA > 2

- Block assessment impossible

- Allergy to local anesthetic

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind


Related Conditions & MeSH terms


Intervention

Procedure:
brachial plexus block

ultrasound guidance

electrical nerve stimulation


Locations

Country Name City State
Norway Department of Anaesthesiology, Rikshospitalet University Hospital Oslo

Sponsors (1)

Lead Sponsor Collaborator
Rikshospitalet University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Block effectiveness, time consumption; patient acceptance, discomfort
See also
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