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COMPLETED NA

Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses

NCT05338333 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to demonstrate noninferiority in visual acuity at distance when wearing the test contact lenses (LID210464) compared to the control contact lenses (AOHG MF) after 30 days of wear.

Conditions Studied

Interventions

  • DEVICE Lehfilcon A multifocal contact lenses
  • DEVICE Lotrafilcon B multifocal contact lenses
  • DEVICE CLEAR CARE®

Study Locations (8)

Florida

  • Kindred Optics at Maitland Vision — Maitland
  • Vision Health Institute — Orlando

Minnesota

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

Kansas

  • Kannarr Eye Care LLC — Pittsburg

Ohio

  • ProCare Vision Centers, Inc. — Granville

Rhode Island

  • West Bay Eye Associates — Warwick

Tennessee

  • Optometry Group, PLLC — Memphis

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2022-05-27
Est. Completion 2022-09-01
Phase NA

Sponsor

Alcon Research

111 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05338333

The ClinicalTrials.gov registry entry for NCT05338333 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 101 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 Presbyopia appearing as the primary indexed condition, and to 3 interventions — of which Lehfilcon A multifocal 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: NCT05338333 reports 8 study locations spanning 6 distinct geographic areas — top geographies include Florida, Minnesota, 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 NCT05338333 about?

NCT05338333 is a clinical study titled "Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses". The primary objective of this study is to demonstrate noninferiority in visual acuity at distance when wearing the test contact lenses (LID210464) compared to the control contact lenses (AOHG MF) after 30 days of wear.

What is the current status of trial NCT05338333?

This trial is currently completed. It is a NA study. The enrollment target is 101 participants. The study started on 2022-05-27. Estimated completion is 2022-09-01.

What conditions does trial NCT05338333 study?

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

What interventions are being tested in trial NCT05338333?

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

Who is sponsoring clinical trial NCT05338333?

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 NCT05338333 being conducted?

This trial has 8 study locations across Florida, Kansas, Minnesota, Ohio, Rhode Island. 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