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COMPLETED NA

Clinical Evaluation of Approved Contact Lenses

NCT02699593 · View on ClinicalTrials.gov ↗

Study Summary

This is a 4-week, randomized, double-masked study where subjects will wear bilaterally test and control lenses in random succession. The objective is to evaluate materials from different suppliers.

Conditions Studied

Interventions

  • DEVICE Test Contact Lens
  • DEVICE Control Contact Lens

Study Locations (7)

Florida

  • Eye Elements Eyecare — Jacksonville
  • Golden Vision — Sarasota

Alabama

  • University of Alabama at Birmingham — Birmingham

Kansas

  • Advantage Eyecare Associates, LLC — Neodesha

Missouri

  • Advanced Eyecare, PC — Raytown

Ohio

  • Professional Vision Care — Westerville

Virginia

  • Timothy R. Poling, OD — Roanoke

Trial Details

FieldValue
Enrollment Target 142 participants
Start Date 2016-02-01
Est. Completion 2016-04-01
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 NCT02699593

The ClinicalTrials.gov registry entry for NCT02699593 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 142 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 Test 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: NCT02699593 reports 7 study locations spanning 6 distinct geographic areas — top geographies include Florida, Alabama, Kansas. 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 NCT02699593 about?

NCT02699593 is a clinical study titled "Clinical Evaluation of Approved Contact Lenses". This is a 4-week, randomized, double-masked study where subjects will wear bilaterally test and control lenses in random succession. The objective is to evaluate materials from different suppliers.

What is the current status of trial NCT02699593?

This trial is currently completed. It is a NA study. The enrollment target is 142 participants. The study started on 2016-02-01. Estimated completion is 2016-04-01.

What conditions does trial NCT02699593 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 NCT02699593?

The interventions under investigation include: Test Contact Lens (DEVICE), Control Contact Lens (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02699593?

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 NCT02699593 being conducted?

This trial has 7 study locations across Alabama, Florida, Kansas, Missouri, 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