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NCT04974697 · ClinicalTrials.gov registry record · NA

Evaluation of Daily Disposable Silicone Hydrogel Multifocal Toric Contact Lenses

A NA study of Visual Acuity, sponsored by Johnson & Johnson Vision Care.

Completed
Registry status
NA
Development phase
95
Enrollment target
8
Study locations

NCT04974697 is a NA study of Visual Acuity that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 95 participants, below the 135-participant average among 20 other Visual Acuity trials with a reported enrollment target (30% lower). The trial reports 8 study locations across 5 states.

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The verdict

NCT04974697, a NA study of Visual Acuity, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
95 participants
Enrollment target
8
Study locations

Study Summary

The study is a bilateral, single-masked, single-arm, 4-visit dispensing study. There will be one study treatment, with the subject being dispensed lenses for 6 to 8 days, then lens power will be optimized (if necessary) and dispensed for a further 2 weeks to assess the clinical performance of investigational multifocal toric contact lenses.

Conditions Studied

Interventions

  • DEVICE JJVC Investigational Multifocal Toric Contact Lens

Study Locations (8)

Florida

  • Stam & Associates Eye Care - Jacksonville
  • VRC-West - Jacksonville
  • Maitland Vision Center - Maitland

New York

  • Eye Associates of New York - New York
  • Sacco Eye Group - Vestal

Kansas

  • Kannarr Eye Care - Pittsburg

Michigan

  • Birmingham Vision Care - Bloomfield Township

Texas

  • Tyler Eye Associates - Tyler

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2021-07-19
Est. Completion 2021-10-29
Phase NA

Sponsor

Johnson & Johnson Vision Care

142 total trials

What the Registry Record Tells You About NCT04974697

The ClinicalTrials.gov registry entry for NCT04974697 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 95 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 135-participant average among 20 other Visual Acuity trials with a reported enrollment target (30% lower). The listed sponsor is Johnson & Johnson Vision Care, which has 142 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Visual Acuity appearing as the primary indexed condition, and to 1 intervention - of which JJVC Investigational Multifocal Toric Contact Lens is the first listed.

NCT04974697 reports 8 study locations spanning 5 distinct geographic areas - top geographies include Florida, New York, Kansas.

Frequently Asked Questions

What is clinical trial NCT04974697 about?

NCT04974697 is a clinical study titled "Evaluation of Daily Disposable Silicone Hydrogel Multifocal Toric Contact Lenses". The study is a bilateral, single-masked, single-arm, 4-visit dispensing study. There will be one study treatment, with the subject being dispensed lenses for 6 to 8 days, then lens power will be optimized (if necessary) and dispensed for a further 2 weeks to assess the clinical performance of invest...

What is the current status of trial NCT04974697?

This trial is currently completed. It is a NA study. The enrollment target is 95 participants. The study started on 2021-07-19. Estimated completion is 2021-10-29.

What conditions does trial NCT04974697 study?

This clinical trial studies the following conditions: Visual Acuity.

What interventions are being tested in trial NCT04974697?

The interventions under investigation include: JJVC Investigational Multifocal Toric Contact Lens (DEVICE).

Who is sponsoring clinical trial NCT04974697?

This trial is sponsored by Johnson & Johnson Vision Care, which has 142 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04974697 being conducted?

This trial has 8 study locations across Florida, Kansas, Michigan, New York, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.