N/A
Completed N=295
Vistakon Investigational Multi-purpose Contact Lens Care Solution.
Contact Lens Wear
Source: ClinicalTrials.gov NCT01055457 ↗
Enrolled (actual)
295
Serious AEs
0.3%
Results posted
Jan 2017
Primary outcomePrimary: Slit Lamp Findings (SLF) — 0; 0; 0; 0 eyes (2 per subject)
Summary
This study compares an investigational contact lens care multi-purpose solution to a currently marketed multi-purpose solution.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Slit Lamp Findings (SLF) |
0; 0; 0; 0; 0; 0 | — |
| PRIMARY Distance Visual Acuity (LogMAR) |
-0.033; -0.042; -0.037; -0.040; -0.029; -0.055 | — |
Eligibility Criteria
Inclusion Criteria
- must be an adapted contact lens wearer
- best corrected distance visual acuity must be 20/25 or better in each eye
- must be wearing their habitual lenses on a daily wear basis
- must be willing to refrain from swimming during the study
Exclusion Criteria
- any systemic diseases that may interfere with contact lens wear
- any clinically significant ocular disease
- any ocular infection
- use of certain medications
- any grade 2 or greater slit lamp findings
- any know sensitivity to marketed contact lens care solutions
- currently pregnant or lactating
- monovision corrected
Data sourced from ClinicalTrials.gov (NCT01055457). 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.