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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 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.
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.
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 109 participants |
| Start Date | 2012-12 |
| Est. Completion | 2013-11 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗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.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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