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COMPLETED NA

The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses

NCT05766787 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.

Conditions Studied

Interventions

  • DEVICE Senofilcon A contact lenses
  • DEVICE CLEAR CARE
  • DEVICE Serafilcon A contact lenses

Study Locations (15)

Florida

  • Omega Vision Center P.A. — Longwood
  • Kindred Optics at Maitland Vision — Maitland
  • Vision Health Institute — Orlando
  • Tallahassee Eye Center — Tallahassee

California

  • Kurata Eyecare Center — Los Angeles
  • Dr. Elsa Pao, OD — Oakland
  • Pacific Rims Optometry — San Francisco

Minnesota

  • The Eye Doctors Inc — Eden Prairie
  • Complete Eye Care of Medina — Medina

Tennessee

  • Optometry Group, PLLC — Memphis
  • Total Eye Care PA — Memphis

Kansas

  • Heart of America Eye Care — Shawnee Mission

New York

  • SUNY College of Optometry Clinical Vision Research Center — New York

Ohio

  • ProCare Vision Centers, Inc. — Granville

Rhode Island

  • West Bay Eye Associates — Warwick

Trial Details

FieldValue
Enrollment Target 190 participants
Start Date 2023-03-29
Est. Completion 2023-06-02
Phase NA

Sponsor

Alcon Research

111 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05766787

The ClinicalTrials.gov registry entry for NCT05766787 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 190 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 Refractive Ametropia appearing as the primary indexed condition, and to 3 interventions — of which Senofilcon 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: NCT05766787 reports 15 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, Minnesota. 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 NCT05766787 about?

NCT05766787 is a clinical study titled "The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses". The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.

What is the current status of trial NCT05766787?

This trial is currently completed. It is a NA study. The enrollment target is 190 participants. The study started on 2023-03-29. Estimated completion is 2023-06-02.

What conditions does trial NCT05766787 study?

This clinical trial studies the following conditions: Refractive Ametropia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05766787?

The interventions under investigation include: Senofilcon A contact lenses (DEVICE), CLEAR CARE (DEVICE), Serafilcon A contact lenses (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05766787?

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 NCT05766787 being conducted?

This trial has 15 study locations across California, Florida, Kansas, Minnesota, New York. 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