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NCT01365039 · ClinicalTrials.gov registry record · NA

Safety and Efficacy of a Contact Lens for Daily Disposable Use

A NA study of Myopia, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
NA
Development phase
173
Enrollment target
1
Study location

NCT01365039 is a NA study of Myopia that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 173 participants, below the 266-participant average among 90 other Myopia trials with a reported enrollment target (35% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01365039, a NA study of Myopia, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
NA
Development phase
173 participants
Enrollment target
1
Study location

Study Summary

This study is to evaluate the safety and efficacy of a new hydrogel daily disposable contact lens compared to the Bausch + Lomb SofLens® daily disposable contact lens when worn by current soft contact lens wearers on a daily disposable wear basis.

Conditions Studied

Myopia

Interventions

  • DEVICE Test, daily disposable contact lens
  • DEVICE SofLens daily disposable contact lens

Study Locations (1)

New York

  • Bausch & Lomb, Inc. - Rochester

Trial Details

FieldValue
Enrollment Target 173 participants
Start Date 2011-06
Est. Completion 2011-10
Phase NA

Sponsor

Bausch & Lomb Incorporated

174 total trials

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What the Registry Record Tells You About NCT01365039

The ClinicalTrials.gov registry entry for NCT01365039 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 173 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 266-participant average among 90 other Myopia trials with a reported enrollment target (35% lower). The listed sponsor is Bausch & Lomb Incorporated, which has 174 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 2 interventions - of which Test, daily disposable contact lens is the first listed.

NCT01365039 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01365039 about?

NCT01365039 is a clinical study titled "Safety and Efficacy of a Contact Lens for Daily Disposable Use". This study is to evaluate the safety and efficacy of a new hydrogel daily disposable contact lens compared to the Bausch + Lomb SofLens® daily disposable contact lens when worn by current soft contact lens wearers on a daily disposable wear basis.

What is the current status of trial NCT01365039?

This trial is currently completed. It is a NA study. The enrollment target is 173 participants. The study started on 2011-06. Estimated completion is 2011-10.

What conditions does trial NCT01365039 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT01365039?

The interventions under investigation include: Test, daily disposable contact lens (DEVICE), SofLens daily disposable contact lens (DEVICE).

Who is sponsoring clinical trial NCT01365039?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01365039 being conducted?

This trial has 1 study location across New York. 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.