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NCT01151371 · ClinicalTrials.gov registry record · NA

Clinical Evaluation Of Two Daily Disposable Contact Lenses And A Monthly Replacement Lens

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

Completed
Registry status
NA
Development phase
452
Enrollment target
20
Study locations

NCT01151371 is a NA study of Myopia that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 452 participants, above the 263-participant average among 90 other Myopia trials with a reported enrollment target (72% higher). The trial reports 20 study locations across 11 states.

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The verdict

NCT01151371, a NA study of Myopia, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
452 participants
Enrollment target
20
Study locations

Study Summary

The objective of the study is to compare the clinical performance of silicone hydrogel daily disposable contact lenses, conventional hydrogel daily disposable contact lenses and silicone hydrogel monthly replacement contact lenses.

Conditions Studied

Interventions

  • DEVICE narafilcon B contact lens
  • DEVICE nelfilcon A contact lens
  • DEVICE lotrafilcon B contact lens

Study Locations (20)

Florida

  • - Jacksonville
  • - Jacksonville
  • - Tampa
  • - Winter Park

California

  • - Brea
  • - Canoga Park
  • - Corona

Missouri

  • - Blue Springs
  • - Independence
  • - Lake Ozark

Ohio

  • - Chagrin Falls
  • - North Olmsted
  • - Warren

Connecticut

  • - Bridgeport

Georgia

  • - Roswell

Indiana

  • - Mishawaka

Massachusetts

  • - Boston

Trial Details

FieldValue
Enrollment Target 452 participants
Start Date 2010-02-01
Est. Completion 2010-04-01
Phase NA

Sponsor

Johnson & Johnson Vision Care

142 total trials

What the Registry Record Tells You About NCT01151371

The ClinicalTrials.gov registry entry for NCT01151371 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 452 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 263-participant average among 90 other Myopia trials with a reported enrollment target (72% higher). 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 Myopia appearing as the primary indexed condition, and to 3 interventions - of which narafilcon B contact lens is the first listed.

NCT01151371 reports 20 study locations spanning 11 distinct geographic areas - top geographies include Florida, California, Missouri.

Frequently Asked Questions

What is clinical trial NCT01151371 about?

NCT01151371 is a clinical study titled "Clinical Evaluation Of Two Daily Disposable Contact Lenses And A Monthly Replacement Lens". The objective of the study is to compare the clinical performance of silicone hydrogel daily disposable contact lenses, conventional hydrogel daily disposable contact lenses and silicone hydrogel monthly replacement contact lenses.

What is the current status of trial NCT01151371?

This trial is currently completed. It is a NA study. The enrollment target is 452 participants. The study started on 2010-02-01. Estimated completion is 2010-04-01.

What conditions does trial NCT01151371 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT01151371?

The interventions under investigation include: narafilcon B contact lens (DEVICE), nelfilcon A contact lens (DEVICE), lotrafilcon B contact lens (DEVICE).

Who is sponsoring clinical trial NCT01151371?

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

Where is trial NCT01151371 being conducted?

This trial has 20 study locations across California, Connecticut, Florida, Georgia, Indiana. 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.