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Clinical Trial Summary

The use of propofol or dexmedetomedine for prevention of sevofurane emergence agitation in LDLT recipients


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 NCT02544906
Study type Interventional
Source Mansoura University
Contact
Status Not yet recruiting
Phase N/A
Start date September 2015
Completion date October 2016

See also
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