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NCT05291936 · ClinicalTrials.gov registry record · NA

Clinical Evaluation of Two Daily Disposable Toric Soft Contact Lenses Over One Week of Wear

A NA study of Ocular Physiology, sponsored by Johnson & Johnson Vision Care.

Completed
Registry status
NA
Development phase
78
Enrollment target
5
Study locations

NCT05291936 is a NA study of Ocular Physiology that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 78 participants. The trial reports 5 study locations across 4 states.

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The verdict

NCT05291936, a NA study of Ocular Physiology, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
78 participants
Enrollment target
5
Study locations

Study Summary

This is a bilateral wear, dispensing, randomized, controlled, double-masked, 2-sequence ×2-period crossover study to evaluate ocular physiology following contact lens wear.

Conditions Studied

Interventions

  • DEVICE PRECISION1® for Astigmatism Contact Lenses
  • DEVICE MyDay® Toric Soft Contact Lenses

Study Locations (5)

Florida

  • VRC - Jacksonville
  • Sabal Eye Care - Longwood

New York

  • Sacco Eye Group - Vestal

Ohio

  • Professional Vision Care Inc. - Westerville - Westerville

Virginia

  • Botetourt Eyecare LLC - Salem

Trial Details

FieldValue
Enrollment Target 78 participants
Start Date 2022-03-30
Est. Completion 2022-05-27
Phase NA

Sponsor

Johnson & Johnson Vision Care

142 total trials

What the Registry Record Tells You About NCT05291936

The ClinicalTrials.gov registry entry for NCT05291936 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 78 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 142 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Ocular Physiology appearing as the primary indexed condition, and to 2 interventions - of which PRECISION1® for Astigmatism Contact Lenses is the first listed.

NCT05291936 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Florida, New York, Ohio.

Frequently Asked Questions

What is clinical trial NCT05291936 about?

NCT05291936 is a clinical study titled "Clinical Evaluation of Two Daily Disposable Toric Soft Contact Lenses Over One Week of Wear". This is a bilateral wear, dispensing, randomized, controlled, double-masked, 2-sequence ×2-period crossover study to evaluate ocular physiology following contact lens wear.

What is the current status of trial NCT05291936?

This trial is currently completed. It is a NA study. The enrollment target is 78 participants. The study started on 2022-03-30. Estimated completion is 2022-05-27.

What conditions does trial NCT05291936 study?

This clinical trial studies the following conditions: Ocular Physiology.

What interventions are being tested in trial NCT05291936?

The interventions under investigation include: PRECISION1® for Astigmatism Contact Lenses (DEVICE), MyDay® Toric Soft Contact Lenses (DEVICE).

Who is sponsoring clinical trial NCT05291936?

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

Where is trial NCT05291936 being conducted?

This trial has 5 study locations across Florida, New York, Ohio, Virginia. 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

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