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Clinical Trial Summary

The purpose of the study is the examine the precision of acceleromyography and mechanomyography during recovery from a neuromuscular blocking agent and to examine whether there is any difference in monitoring block at the dominant or non-dominant arm. Our hypothesis is that there is no significant difference in neither the precision nor the level of block in the contralateral arms.


Clinical Trial Description

n/a


Study Design

N/A


Related Conditions & MeSH terms


NCT number NCT00472121
Study type Observational
Source Rigshospitalet, Denmark
Contact
Status Completed
Phase Phase 4
Start date May 2007
Completion date October 2007

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