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COMPLETED NA

Clinical Evaluation of a Reusable Multifocal Optical Design in a Presbyopic Population Phase 2

NCT03586648 · View on ClinicalTrials.gov ↗

Study Summary

This is a single-masked, randomized-controlled, dispensing clinical trial. A total of approximately 60 eligible hyperopic subjects will be targeted to complete this study.

Conditions Studied

Interventions

  • DEVICE senofilcon A Multifocal
  • DEVICE senofilcon A Sphere
  • DEVICE etafilcon A Multifocal
  • DEVICE etafilcon A Sphere

Study Locations (6)

Florida

  • Dr. James E. Weber — Jacksonville
  • Maitland Vision Center — Maitland
  • Wayne Golden, OD — Sarasota

Ohio

  • Western Reserve Vision Care — Beechwood
  • Procare Vision Center — Granville

California

  • Golden Optometric Group — Whittier

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2018-06-14
Est. Completion 2018-08-20
Phase NA

Sponsor

Johnson & Johnson Vision Care

36 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03586648

The ClinicalTrials.gov registry entry for NCT03586648 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 71 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 4 interventions — of which senofilcon A Multifocal 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: NCT03586648 reports 6 study locations spanning 3 distinct geographic areas — top geographies include Florida, Ohio, California. 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 NCT03586648 about?

NCT03586648 is a clinical study titled "Clinical Evaluation of a Reusable Multifocal Optical Design in a Presbyopic Population Phase 2". This is a single-masked, randomized-controlled, dispensing clinical trial. A total of approximately 60 eligible hyperopic subjects will be targeted to complete this study.

What is the current status of trial NCT03586648?

This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2018-06-14. Estimated completion is 2018-08-20.

What conditions does trial NCT03586648 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 NCT03586648?

The interventions under investigation include: senofilcon A Multifocal (DEVICE), senofilcon A Sphere (DEVICE), etafilcon A Multifocal (DEVICE), etafilcon A Sphere (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03586648?

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 NCT03586648 being conducted?

This trial has 6 study locations across California, Florida, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial