Contact Lens Complication Clinical Trial
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™
NCT number | NCT02298400 |
Other study ID # | 14-270-0001 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2014 |
Est. completion date | September 2014 |
Verified date | April 2024 |
Source | ORA, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the comfort of three commercially available contact lenses.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2014 |
Est. primary completion date | September 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Be at least 18 years old - Have provided written informed consent - Have discomfort when wearing contact lenses Exclusion Criteria: - Have an active ocular infection or significant slit lamp findings - Participated in any other studies in the past 30 days |
Country | Name | City | State |
---|---|---|---|
United States | Andover Eye Associates | Andover | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
ORA, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Contact lens wear comfort, as assessed by subject reported symptoms in diaries. | 1 week |
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