N/A
Completed N=30
Evaluation of Wear Experience With a Water Surface Daily Disposable Contact Lens
Contact Lens
Source: ClinicalTrials.gov NCT05102383 ↗
Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Dec 2023
Primary outcomePrimary: Subjective Assessment of Overall Comfort With Verofilcon A Daily Disposable Lenses for Astigmatism — 91 units on a scale
Summary
The purpose of this study is to assess the wear experience of existing wearers of a monthly replacement contact lens after they have been fit with a daily disposable contact lens that has water surface treatment.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Subjective Assessment of Overall Comfort With Verofilcon A Daily Disposable Lenses for Astigmatism |
91 | — |
Eligibility Criteria
Inclusion Criteria
- Must be a current wearer of Comfilcon A contact lenses
- Distance visual acuity of 20/25 or better with current contact lenses
- Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI)
- Ability to give informed consent
- Willing to spend time for the study, which includes attending three study visits and be willing to wear contact lenses on days between study visits.
- Either gender.
- Any racial or ethnic origin.
Exclusion Criteria
- No current ocular inflammation or infection.
- Not currently pregnant or lactating
Data sourced from ClinicalTrials.gov (NCT05102383). 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.