Viewing Study NCT00366769


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Study NCT ID: NCT00366769
Status: COMPLETED
Last Update Posted: 2006-08-21
First Post: 2006-08-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Evaluation of Outcomes Following LASIK Surgery Using CustomVue
Sponsor: Medical University of South Carolina
Organization:

Study Overview

Official Title: Evaluation of Visual Outcomes, Contrast Sensitivity, Glare, and Induction of High Order Aberrations Following LASIK Surgery Using CustomVue
Status: COMPLETED
Status Verified Date: 2006-03
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 aim of the study was to evaluate visual outcomes, contrast sensitivity, glare and induced high order aberrations induced by the new CustomVue software use for wavefront-guided LASIK.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: