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Clinical Evaluation of a Daily Wear Reusable Multifocal Optical Design in a Presbyopic Population
NCT04534517 · View on ClinicalTrials.gov ↗
Study Summary
The clinical study is a bilateral, single-masked (partial), single-arm, clinical trial. A total of approximately 60 eligible subjects both near-sighted and far-sighted, will be targeted to complete the study. Subjects will be fit in the study lens for approximately 2-4 days then undergo lens optimization, if required. Subjects will then be given a new pair of lenses that will be worn for approximately 2 weeks.
Conditions Studied
Interventions
- DEVICE JJV Investigational Multifocal Contact Lens
- DEVICE ACUVUE OASYS® with HYDRACLEAR® PLUS
Study Locations (11)
Florida
- Dr. James Weber & Associates, PA — Jacksonville
- Sabal Eye Care — Longwood
- Maitland Vision Center — Maitland
Georgia
- VisualEyes — Roswell
Illinois
- VisionPoint Eye Center — Bloomington
Kansas
- Kannarr Eye Care — Pittsburg
Missouri
- Advanced Eyecare — Raytown
New York
- Sacco Eye Group — Vestal
Ohio
- ProCare Vision Centers — Granville
Rhode Island
- Dr. David W. Ferris & Associates — Warwick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 119 participants |
| Start Date | 2020-08-07 |
| Est. Completion | 2020-09-29 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04534517
The ClinicalTrials.gov registry entry for NCT04534517 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 119 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 JJV Investigational Multifocal Contact Lens 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: NCT04534517 reports 11 study locations spanning 9 distinct geographic areas — top geographies include Florida, Georgia, 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 NCT04534517 about?
NCT04534517 is a clinical study titled "Clinical Evaluation of a Daily Wear Reusable Multifocal Optical Design in a Presbyopic Population". The clinical study is a bilateral, single-masked (partial), single-arm, clinical trial. A total of approximately 60 eligible subjects both near-sighted and far-sighted, will be targeted to complete the study. Subjects will be fit in the study lens for approximately 2-4 days then undergo lens optimiz...
What is the current status of trial NCT04534517?
This trial is currently completed. It is a NA study. The enrollment target is 119 participants. The study started on 2020-08-07. Estimated completion is 2020-09-29.
What conditions does trial NCT04534517 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 NCT04534517?
The interventions under investigation include: JJV Investigational Multifocal Contact Lens (DEVICE), ACUVUE OASYS® with HYDRACLEAR® PLUS (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04534517?
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 NCT04534517 being conducted?
This trial has 11 study locations across Florida, Georgia, Illinois, Kansas, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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