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

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The contact lens was aseptically removed from the eye. Lipids were extracted and analyzed using a proprietary High Performance Liquid Chromatography technique. A lower value indicates a cleaner lens surface. One eye (study eye) contributed to the mean.

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
Alcon Research

275 total trials

What the finished NCT01699750 record still lists

NCT01699750 is an interventional study that assigns participants to a tested intervention. The registered 109 participants enrollment target is mid-sized for trials with a published cap, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (59% lower).

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 a single indexed study location in 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.

Where NCT01699750's enrollment target sits among peer trials

109 37th of 90 higher than 54 of 90 other Myopia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Myopia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01699750, the US trial registry maintained by the National Library of Medicine. NCT01699750 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.