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Clinical Trial Summary

The purpose of this study is to determine the incidence of post-operative residual curarization in our patients and to determine if Cisatracurium and Rocuronium behave differently from each other in terms of residual curarization.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01651572
Study type Interventional
Source Azienda Ospedaliera di Padova
Contact
Status Completed
Phase Phase 4
Start date July 2012
Completion date July 2013

See also
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