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Clinical Evaluation of Reusable Soft Contact Lenses
NCT06119191 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study was to confirm the clinical performance of a novel manufacturing process for comfilcon A contact lenses in habitual wearers over a one-month period of lens wear.
Conditions Studied
Interventions
- DEVICE Control Lenses (comfilcon A with current process)
- DEVICE Test Lenses (comfilcon A with novel process)
Study Locations (5)
Ohio
- Ohio State University College of Optometry — Columbus
- ProCare Vision Center, Inc. — Granville
California
- Clinical Research Center, UC Berkeley — Berkeley
Indiana
- Clinical Optics Research Lab at IU School of Optometry — Bloomington
New York
- SUNY College of Optometry Clinical Vision Research Center — New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 77 participants |
| Start Date | 2023-11-14 |
| Est. Completion | 2024-03-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06119191
The ClinicalTrials.gov registry entry for NCT06119191 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 77 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CooperVision International Limited (CVIL), which has 4 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 2 interventions — of which Control Lenses (comfilcon A with current process) 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: NCT06119191 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Ohio, California, Indiana. 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 NCT06119191 about?
NCT06119191 is a clinical study titled "Clinical Evaluation of Reusable Soft Contact Lenses". The purpose of this study was to confirm the clinical performance of a novel manufacturing process for comfilcon A contact lenses in habitual wearers over a one-month period of lens wear.
What is the current status of trial NCT06119191?
This trial is currently completed. It is a NA study. The enrollment target is 77 participants. The study started on 2023-11-14. Estimated completion is 2024-03-01.
What conditions does trial NCT06119191 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 NCT06119191?
The interventions under investigation include: Control Lenses (comfilcon A with current process) (DEVICE), Test Lenses (comfilcon A with novel process) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06119191?
This trial is sponsored by CooperVision International Limited (CVIL), which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06119191 being conducted?
This trial has 5 study locations across California, Indiana, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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