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NCT01412983 · ClinicalTrials.gov registry record · NA

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens

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

Completed
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT01412983 is a NA study of Myopia that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 100 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01412983, a NA study of Myopia, has completed, sponsored by Bausch & Lomb Incorporated.

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

Study Summary

The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses developed by Bausch + Lomb.

Conditions Studied

Myopia

Interventions

  • DEVICE Bausch & Lomb Test lens
  • DEVICE Ciba Vision soft contact lens

Study Locations (1)

New York

  • Bausch & Lomb Incorporated - Rochester

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2011-08
Est. Completion 2011-10
Phase NA

Sponsor

Bausch & Lomb Incorporated

174 total trials

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What the Registry Record Tells You About NCT01412983

The ClinicalTrials.gov registry entry for NCT01412983 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (63% 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 Bausch & Lomb Test lens is the first listed.

NCT01412983 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01412983 about?

NCT01412983 is a clinical study titled "A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens". The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses developed by Bausch + Lomb.

What is the current status of trial NCT01412983?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2011-08. Estimated completion is 2011-10.

What conditions does trial NCT01412983 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT01412983?

The interventions under investigation include: Bausch & Lomb Test lens (DEVICE), Ciba Vision soft contact lens (DEVICE).

Who is sponsoring clinical trial NCT01412983?

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

Where is trial NCT01412983 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.