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Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens
NCT04476784 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the clinical performance of an investigational contact lens over 30 days of daily wear.
Conditions Studied
Interventions
- DEVICE Comfilcon A contact lenses
- DEVICE Lehfilcon A contact lenses
- DEVICE CLEAR CARE
Study Locations (5)
Kansas
- Alcon Investigative Site — Pittsburg
- Alcon Investigative Site — Shawnee Mission
Florida
- Alcon Investigative Site — Maitland
Illinois
- Alcon Investigative Site — Bloomington
Tennessee
- Alcon Investigative Site — Memphis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2020-08-17 |
| Est. Completion | 2020-11-18 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04476784
The ClinicalTrials.gov registry entry for NCT04476784 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 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 111 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 appearing as the primary indexed condition, and to 3 interventions — of which Comfilcon A contact lenses 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: NCT04476784 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Kansas, Florida, 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 NCT04476784 about?
NCT04476784 is a clinical study titled "Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens". The purpose of this study is to assess the clinical performance of an investigational contact lens over 30 days of daily wear.
What is the current status of trial NCT04476784?
This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2020-08-17. Estimated completion is 2020-11-18.
What conditions does trial NCT04476784 study?
This clinical trial studies the following conditions: Myopia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04476784?
The interventions under investigation include: Comfilcon A contact lenses (DEVICE), Lehfilcon A contact lenses (DEVICE), CLEAR CARE (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04476784?
This trial is sponsored by Alcon Research, which has 111 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04476784 being conducted?
This trial has 5 study locations across Florida, Illinois, Kansas, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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