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Dispensing Evaluation of Investigational Contact Lenses
NCT02625220 · View on ClinicalTrials.gov ↗
Study Summary
Non-randomized, single-masked, 2-visit, bilateral wear, single-arm dispensing study to evaluate the visual acuity, rotational performance, lens fit, stability and subjective characteristics of a senofilcon-based JJVCI investigational toric contact lens design.
Conditions Studied
Interventions
- DEVICE Prototype toric lens senofilcon A
Study Locations (12)
Florida
- Edward S. Wygonik, OD — Jacksonville
- The Eye Center — Pembroke Pines
- Eye Associates of Winter Park — Winter Park
Ohio
- New Image Eye Center — Springfield
- Professional Vision Care — Westerville
Illinois
- Eyecare Associates — Bloomington
Indiana
- Indiana University College of Optometry — Bloomington
Kansas
- Kannarr Eye Care — Pittsburg
New Mexico
- ABQ Eyecare — Albuquerque
New York
- Sacco Eye Group — Vestal
Rhode Island
- West Bay Eye Associates — Warwick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 177 participants |
| Start Date | 2015-10 |
| Est. Completion | 2015-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02625220
The ClinicalTrials.gov registry entry for NCT02625220 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 177 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Vision Care, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Myopia; Astigmatism appearing as the primary indexed condition, and to 1 intervention — of which Prototype toric lens senofilcon A is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02625220 reports 12 study locations spanning 9 distinct geographic areas — top geographies include Florida, Ohio, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02625220 about?
NCT02625220 is a clinical study titled "Dispensing Evaluation of Investigational Contact Lenses". Non-randomized, single-masked, 2-visit, bilateral wear, single-arm dispensing study to evaluate the visual acuity, rotational performance, lens fit, stability and subjective characteristics of a senofilcon-based JJVCI investigational toric contact lens design.
What is the current status of trial NCT02625220?
This trial is currently completed. It is a NA study. The enrollment target is 177 participants. The study started on 2015-10. Estimated completion is 2015-11.
What conditions does trial NCT02625220 study?
This clinical trial studies the following conditions: Myopia; Astigmatism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02625220?
The interventions under investigation include: Prototype toric lens senofilcon A (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02625220?
This trial is sponsored by Johnson & Johnson Vision Care, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02625220 being conducted?
This trial has 12 study locations across Florida, Illinois, Indiana, Kansas, New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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