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NCT03787472 · ClinicalTrials.gov registry record · NA

Clinical Evaluation of Manufacturing Processes for a Reusable Multifocal Optical Design in a Presbyopic Population

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

Completed
Registry status
NA
Development phase
45
Enrollment target
5
Study locations

NCT03787472 is a NA study of Visual Acuity that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 45 participants, below the 138-participant average among 20 other Visual Acuity trials with a reported enrollment target (67% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT03787472, a NA study of Visual Acuity, has completed, sponsored by Johnson & Johnson Vision Care.

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

Study Summary

The clinical study is a randomized-controlled, double-masked, crossover clinical trial with two study treatments to compare two study lens types and the initial performance, in terms of the subjective response after a period of lens dispensing. The study will last approximately 2 to 4 months.

Conditions Studied

Interventions

  • DEVICE JJV Investigational senofilcon A Multifocal Lens1
  • DEVICE JJV Investigational senofilcon A Multifocal Lens2

Study Locations (5)

Ohio

  • Western Reserve Vision Care, Inc - Beachwood
  • ProCare Vision Centers - Granville

Florida

  • Maitland Vision Center - Maitland

Missouri

  • Advanced Eyecare - Raytown

New York

  • Spectrum Eyecare - Jamestown

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2019-01-11
Est. Completion 2019-03-22
Phase NA

Sponsor

Johnson & Johnson Vision Care

142 total trials

What the Registry Record Tells You About NCT03787472

The ClinicalTrials.gov registry entry for NCT03787472 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 138-participant average among 20 other Visual Acuity trials with a reported enrollment target (67% 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 2 interventions - of which JJV Investigational senofilcon A Multifocal Lens1 is the first listed.

NCT03787472 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Ohio, Florida, Missouri.

Frequently Asked Questions

What is clinical trial NCT03787472 about?

NCT03787472 is a clinical study titled "Clinical Evaluation of Manufacturing Processes for a Reusable Multifocal Optical Design in a Presbyopic Population". The clinical study is a randomized-controlled, double-masked, crossover clinical trial with two study treatments to compare two study lens types and the initial performance, in terms of the subjective response after a period of lens dispensing. The study will last approximately 2 to 4 months.

What is the current status of trial NCT03787472?

This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2019-01-11. Estimated completion is 2019-03-22.

What conditions does trial NCT03787472 study?

This clinical trial studies the following conditions: Visual Acuity.

What interventions are being tested in trial NCT03787472?

The interventions under investigation include: JJV Investigational senofilcon A Multifocal Lens1 (DEVICE), JJV Investigational senofilcon A Multifocal Lens2 (DEVICE).

Who is sponsoring clinical trial NCT03787472?

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

Where is trial NCT03787472 being conducted?

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