N/A
Completed N=55
Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2
Source: ClinicalTrials.gov NCT04528017 ↗Enrolled (actual)
55
Serious AEs
0.0%
Results posted
Nov 2021
Primary outcomePrimary: Distance Visual Acuity (VA) With Study Lenses — -0.13; -0.15 logMAR
Summary
The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Clariti 1-Day contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Distance Visual Acuity (VA) With Study Lenses |
-0.13; -0.15 | — |
Eligibility Criteria
Key Inclusion Criteria
- Subject must be able to understand and must sign an Institution Review Board (IRB) approved Informed Consent Form.
- Successful wear of soft contact lenses in both eyes for a minimum of 5 days per week and 10 hours per day during the past 3 months.
- Willing to wear contact lenses for at least 16 hours per day on one of the days with each lens type.
- Other protocol-specified inclusion criteria may apply.
Key Exclusion Criteria
- Any ocular condition that contraindicates contact lens wear.
- Previous or current habitual wearer of PRECISION1, Clariti 1-Day, or DAILIES TOTAL1 contact lenses.
- Other protocol-specified exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT04528017). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.