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Clinical Trial Summary

The aim of this study was to compare the intraoperative efficiency, safety and postoperative outcomes of cataract surgery with two different "high-fluidic" settings.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


NCT number NCT01936714
Study type Interventional
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date February 2013
Completion date September 2013

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