North American Comfilcon A Clinical Study
Condition(s) studied
Investigational drug(s) / intervention(s)
comfilcon A Sphere lens: 2 hours of wear
comfilcon A Toric lens: 2 hours of wear
comfilcon A Multifocal lens: 2 hours of wear
comfilcon A Multifocal Toric lens: 2 hours of wear
comfilcon A Energys lens: 2 hours of wear
Study summary
The main objective of this study is to demonstrate acceptable safety and effectiveness (performance) of comfilcon A Sphere, Toric, Multifocal, Toric Multifocal and Energys lenses, when used in the general population.
Eligibility
Primary outcome measure(s)
- Visual Performance (Visual Acuity) — At the end of 2 hours of wear
Visual Performance will be measured using logMAR * High contrast, high illumination distance VA * High contrast, high illumination near VA - Incidence of contact lens-related adverse events — At the end of 2 hours of wear
Incidence of contact lens-related adverse events will be recorded from subjects
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| University of Berkeley | Berkeley | California | |
| ProCare Vision Center | Granville | Ohio | |
| Nittany Eye Associates | College | Pennsylvania | |
| Drs. McIntyre, Garza, Avila and Jurica, Optometrists | Corpus Christi | Texas |
More CooperVision International Limited (CVIL) trials in the USA
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06902584 on ClinicalTrials.gov ↗ ← All trials in the USA