N/A
Completed N=36
Clinical Assessment of Two Daily Wear Reusable Soft Silicone Hydrogel Contact Lenses
Source: ClinicalTrials.gov NCT05056987 ↗Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcomePrimary: Distance VA (logMAR) With Study Lenses — -0.08; -0.10; -0.07; -0.07 logMAR
Summary
The overall objective of this clinical study is to describe the clinical performance of the TOTAL30® soft contact lens compared to the ACUVUE® OASYS® with HYDRACLEAR PLUS (AOHP) soft contact lens in a daily wear modality.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Distance VA (logMAR) With Study Lenses |
-0.08; -0.10; -0.07; -0.07 | — |
Eligibility Criteria
Key Inclusion Criteria
- Currently wearing any commercial spherical soft contact lenses with at least 3 months wearing experience.
- Willing to wear the study lenses for a minimum of 5 days per week and 8 hours per day.
- Willing to NOT use rewetting/lubricating drops at any time during the study.
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria
- Participation in a clinical trial within the previous 14 days or currently enrolled in any clinical trial.
- Habitual AOHP contact lens wearers (in the past 3 months).
- Monovision wear during the study.
- Other protocol-defined exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT05056987). 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.