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Clinical Trial Summary

To explore the feasibility of different doses of etomidate admixed with propofol in induced abortion: a randomized, double blind controlled trial.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT02208596
Study type Interventional
Source Third Affiliated Hospital of Zhengzhou University
Contact
Status Not yet recruiting
Phase Phase 4
Start date September 2014
Completion date February 2015

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