Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01699750 · ClinicalTrials.gov registry record · NA

Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems

A NA study of Myopia and Astigmatism, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
109
Enrollment target
1
Study location

NCT01699750 is a NA study of Myopia and Astigmatism that has completed, run by Alcon Research. The registered enrollment target is 109 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (59% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01699750, a NA study of Myopia and Astigmatism, has completed, sponsored by Alcon Research.

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

Study Summary

The purpose of this study is to evaluate the lipid uptake, wetting characteristics, and visual performance of AIR OPTIX® AQUA and ACUVUE® OASYS® with HYDRACLEAR® contact lenses when used in conjunction with two contact lens care systems.

Interventions

  • DEVICE Lotrafilcon B contact lenses
  • DEVICE Senofilcon A contact lenses
  • DEVICE OPTI-FREE® PUREMOIST® MPDS
  • DEVICE BIOTRUE®
  • DEVICE Balafilcon A contact lenses

Study Locations (1)

Texas

  • Contact Alcon Call Center at 1-888-451-3937 for Trial Locations - Fort Worth

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2012-12
Est. Completion 2013-11
Phase NA

Sponsor

Alcon Research

275 total trials

What the Registry Record Tells You About NCT01699750

The ClinicalTrials.gov registry entry for NCT01699750 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 109 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 (59% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Myopia appearing as the primary indexed condition, and to 5 interventions - of which Lotrafilcon B contact lenses is the first listed.

NCT01699750 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT01699750 about?

NCT01699750 is a clinical study titled "Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems". The purpose of this study is to evaluate the lipid uptake, wetting characteristics, and visual performance of AIR OPTIX® AQUA and ACUVUE® OASYS® with HYDRACLEAR® contact lenses when used in conjunction with two contact lens care systems.

What is the current status of trial NCT01699750?

This trial is currently completed. It is a NA study. The enrollment target is 109 participants. The study started on 2012-12. Estimated completion is 2013-11.

What conditions does trial NCT01699750 study?

This clinical trial studies the following conditions: Myopia, Astigmatism, Refractive Error.

What interventions are being tested in trial NCT01699750?

The interventions under investigation include: Lotrafilcon B contact lenses (DEVICE), Senofilcon A contact lenses (DEVICE), OPTI-FREE® PUREMOIST® MPDS (DEVICE), BIOTRUE® (DEVICE), Balafilcon A contact lenses (DEVICE).

Who is sponsoring clinical trial NCT01699750?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01699750 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Myopia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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.