Viewing Study NCT02298400


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Study NCT ID: NCT02298400
Status: WITHDRAWN
Last Update Posted: 2024-04-25
First Post: 2014-11-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses
Sponsor: ORA, Inc.
Organization:

Study Overview

Official Title: A Single-Center, Cross-over, Pilot Study Evaluating Acuvue® Oasys® Lenses (Senofilcon A), 30-Day Bausch + Lomb PureVision (Balafilcon A), and Clariti® 1-Day (Somofilcon A) Lenses, for Their Impact on Ocular Discomfort Induced by Exposure to the Turbo Controlled Adverse Environment™
Status: WITHDRAWN
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study terminated by Sponsor
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 compare the comfort of three commercially available contact lenses.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: