Viewing Study NCT01061294



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Last Modification Date: 2024-10-26 @ 10:15 AM
Study NCT ID: NCT01061294
Status: COMPLETED
Last Update Posted: 2011-01-13
First Post: 2010-02-01

Brief Title: Evaluation of Outcomes Using the AMO Advanced Customvue iLasik Procedure
Sponsor: Innovative Medical
Organization: Innovative Medical

Study Overview

Official Title: Evaluation of Outcomes Using the AMO Advanced Customvue iLasik Procedure Wavescan Wavefront System Star S4 IR Excimer Laser System and Intralse FS System
Status: COMPLETED
Status Verified Date: 2011-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the efficacy predictability and safety of the Advanced CustomVue iLASIK procedure WaveScan WaveFront System STAR S4 IR Excimer Laser System and IntraLase FS System Patient data will be collected electronically and analyzed to determine improvements in postoperative visual acuity visual quality and residual error
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None