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Clinical Trial Summary

Main objective is to evaluate the sparing effect of esmolol on the required doses of propofol and remifentanil


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00922467
Study type Interventional
Source Hopital Foch
Contact
Status Terminated
Phase Phase 3
Start date June 2009
Completion date December 2011

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