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NCT01309867 · ClinicalTrials.gov registry record · NA

A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses

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

Completed
Registry status
NA
Development phase
302
Enrollment target
1
Study location

NCT01309867 is a NA study of Myopia that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 302 participants, above the 265-participant average among 90 other Myopia trials with a reported enrollment target (14% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT01309867, a NA study of Myopia, has completed, sponsored by Bausch & Lomb Incorporated.

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

Study Summary

The objective of the study is to evaluate the product performance of the Bausch + Lomb toric investigational contact lenses compared to the currently marketed PureVision toric contact lenses.

Conditions Studied

Myopia

Interventions

  • DEVICE Investigational Toric Lens
  • DEVICE PureVision Toric Lens

Study Locations (1)

New York

  • Bausch & Lomb - Rochester

Trial Details

FieldValue
Enrollment Target 302 participants
Start Date 2010-12
Est. Completion 2011-04
Phase NA

Sponsor

Bausch & Lomb Incorporated

174 total trials

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What the Registry Record Tells You About NCT01309867

The ClinicalTrials.gov registry entry for NCT01309867 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 302 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 265-participant average among 90 other Myopia trials with a reported enrollment target (14% higher). 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 Investigational Toric Lens is the first listed.

NCT01309867 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01309867 about?

NCT01309867 is a clinical study titled "A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses". The objective of the study is to evaluate the product performance of the Bausch + Lomb toric investigational contact lenses compared to the currently marketed PureVision toric contact lenses.

What is the current status of trial NCT01309867?

This trial is currently completed. It is a NA study. The enrollment target is 302 participants. The study started on 2010-12. Estimated completion is 2011-04.

What conditions does trial NCT01309867 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT01309867?

The interventions under investigation include: Investigational Toric Lens (DEVICE), PureVision Toric Lens (DEVICE).

Who is sponsoring clinical trial NCT01309867?

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

Where is trial NCT01309867 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.