N/A
Completed N=60
Clinical Comparison of Two Daily Disposable Contact Lenses - Pilot Study 3
Source: ClinicalTrials.gov NCT04942925 ↗Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Sep 2022
Primary outcomePrimary: Distance VA (logMAR) With Study Lenses — -0.14; -0.15 logMAR
Summary
The purpose of this study is to evaluate the overall performance of PRECISION1™ contact lenses when compared to INFUSE™ contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Distance VA (logMAR) With Study Lenses |
-0.14; -0.15 | — |
Eligibility Criteria
Key Inclusion Criteria
- Able to understand and sign an Informed Consent Form that been approved by an Institutional Review Board.
- Successful wear of spherical soft contact lenses in both eyes for a minimum of 5 days per week and 10 hours per day during the past 3 months.
- Other protocol-defined inclusion criteria may apply.
Key Exclusion Criteria
- Current/previous PRECISION1 or INFUSE contact lens wearer.
- Any eye condition or use of medication that contraindicates contact lens wear, as determined by the investigator.
- Routinely sleeps in contact lenses.
- Other protocol-defined exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT04942925). 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.