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Assisted Nerve Blocks

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Thomas Hemmerling, McGill University Health Center
ClinicalTrials.gov Identifier:
NCT01436682
First received: September 19, 2011
Last updated: October 24, 2013
Last verified: October 2013
September 19, 2011
October 24, 2013
September 2011
August 2013   (Final data collection date for primary outcome measure)
Feasability of assisted nerve blocks [ Time Frame: 24h ]
Not Provided
Complete list of historical versions of study NCT01436682 on ClinicalTrials.gov Archive Site
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Assisted Nerve Blocks
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The study investigates assisted nerve blocks using an ultrasound machine.
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Observational
Observational Model: Case Control
Time Perspective: Prospective
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Non-Probability Sample
Patient undergoing surgery which necessitates a peripheral nerve block to relieve postoperative pain.
Surgery
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
13
August 2013
August 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • indication for nerve blocks

Exclusion Criteria:

  • patient not able to provide the informed consent
  • allergy to local anesthetics
Sexes Eligible for Study: All
18 Years to 90 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
 
NCT01436682
GEN11-073
No
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Thomas Hemmerling, McGill University Health Center
McGill University Health Center
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McGill University Health Center
October 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP