Clinical Validation of DACP Digital Design
Completed · Not applicable
Conditions studied: Refractive Errors
In brief
The purpose of this study is to evaluate the visual performance of DAILIES® AquaComfort Plus® (DACP) Digital lenses by assessing distance visual acuity (VA) as compared to DACP sphere contact lenses after one week of wear.
Key facts
- Study ID
- NCT03567005
- Run by
- Alcon Research
- People needed
- 60
- Starts
- 2018-06-25
- Expected to finish
- 2018-08-26
- Last updated by the study team
- 2019-06-18
Who can join
Age: 18 and older, up to 35. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Willing and able to sign an IRB/IEC approved Informed Consent form;
- Current wearer of DACP spherical contact lenses (at least 2 months in current correction), with a minimum wearing time of 5 days per week and 8 hours per day;
- Experiencing symptoms of eye strain from using technology;
- Willing to wear study lenses each day;
- Possess spectacles that provide a corrected visual acuity of 20/40 or better in both eyes (OU) and be willing to wear them (as needed);
- Willing to NOT use rewetting/lubricating drops at any time during the study;
- Currently using digital devices (computer, tablet, and/or smart phone) for a minimum of 5 days per week and 4 hours per day;
- Willing to NOT use any near aid (e.g. reading glasses) at any time during the study.
You may not qualify if…
- Conditions, use of medications, injury, or surgery, as specified in the protocol;
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment;
- Monocular (only one eye with functional vision);
- Pregnant.
Where it is running
- Alcon Investigative Site — Bloomington, Illinois, United States
- Alcon Investigative Site — Powell, Ohio, United States
- Alcon Investigative Site — Brentwood, Tennessee, United States
- Alcon Investigative Site — Memphis, Tennessee, United States
- Alcon Investigative Site — Memphis, Tennessee, United States
Full record on ClinicalTrials.gov
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