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Evaluation of Dryness in a Silicone Hydrogel Daily Disposable Contact Lens
NCT04849780 · View on ClinicalTrials.gov ↗
Study Summary
This is a multi-site, randomized, bilateral, dispensing, parallel design study with two arms to evaluate contact lens related dry eye symptoms and subjective comfort.
Conditions Studied
Interventions
- DEVICE ACUVUE Oasys 1-Day
- DEVICE Habitual Lens
Study Locations (9)
Florida
- Vue Optical Boutique — Jacksonville
- Sabal Eye Care — Longwood
- Maitland Vision Center — Maitland
Kansas
- Kannarr Eye Care — Pittsburg
New York
- Sacco Eye Group — Vestal
Ohio
- Procare Vision Centers — Granville
Rhode Island
- Dr. David Ferris & Associates — Warwick
Tennessee
- Optometry Group Pllc — Memphis
Texas
- Tyler Eye Associates — Tyler
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 95 participants |
| Start Date | 2021-04-17 |
| Est. Completion | 2021-08-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04849780
The ClinicalTrials.gov registry entry for NCT04849780 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 95 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 Visual Acuity appearing as the primary indexed condition, and to 2 interventions — of which ACUVUE Oasys 1-Day 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: NCT04849780 reports 9 study locations spanning 7 distinct geographic areas — top geographies include Florida, Kansas, New York. 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 NCT04849780 about?
NCT04849780 is a clinical study titled "Evaluation of Dryness in a Silicone Hydrogel Daily Disposable Contact Lens". This is a multi-site, randomized, bilateral, dispensing, parallel design study with two arms to evaluate contact lens related dry eye symptoms and subjective comfort.
What is the current status of trial NCT04849780?
This trial is currently completed. It is a NA study. The enrollment target is 95 participants. The study started on 2021-04-17. Estimated completion is 2021-08-12.
What conditions does trial NCT04849780 study?
This clinical trial studies the following conditions: Visual Acuity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04849780?
The interventions under investigation include: ACUVUE Oasys 1-Day (DEVICE), Habitual Lens (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04849780?
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 NCT04849780 being conducted?
This trial has 9 study locations across Florida, Kansas, New York, Ohio, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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