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Clinical Assessment of a HYDRAGLYDE® Regimen
NCT03026257 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate worn AIR OPTIX® plus HYDRAGLYDE® (AOHG) lenses cleaned and disinfected with HYDRAGLYDE® containing lens solutions compared to each of the control habitual silicone hydrogel (SiHy) lenses cleaned and disinfected with habitual multi-purpose solution (MPS) for cholesterol uptake.
Conditions Studied
Interventions
- DEVICE Lotrafilcon B contact lenses with added wetting agent
- DEVICE Samfilcon A contact lenses
- DEVICE POLYQUAD/ALDOX-preserved contact lens solution with added wetting agent
- DEVICE Hydrogen peroxide-based contact lens solution with added wetting agent
- DEVICE Senofilcon C contact lenses
Study Locations (8)
Ohio
- Alcon Investigative Site — Cleveland
- Alcon Investigative Site — Columbus
Other
- Alcon Investigative Site — Hildesheim
- Alcon Investigative Site — Jena
Alabama
- Alcon Investigative Site — Birmingham
Tennessee
- Alcon Investigative Site — Memphis
Texas
- Alcon Investigative Site — Houston
Ontario
- Alcon Investigative Site — Waterloo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 323 participants |
| Start Date | 2017-02-13 |
| Est. Completion | 2017-08-18 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03026257
The ClinicalTrials.gov registry entry for NCT03026257 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 323 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon, a Novartis Company, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Myopia appearing as the primary indexed condition, and to 5 interventions — of which Lotrafilcon B contact lenses with added wetting agent is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03026257 reports 8 study locations spanning 6 distinct geographic areas — top geographies include Ohio, Other, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03026257 about?
NCT03026257 is a clinical study titled "Clinical Assessment of a HYDRAGLYDE® Regimen". The purpose of this study is to evaluate worn AIR OPTIX® plus HYDRAGLYDE® (AOHG) lenses cleaned and disinfected with HYDRAGLYDE® containing lens solutions compared to each of the control habitual silicone hydrogel (SiHy) lenses cleaned and disinfected with habitual multi-purpose solution (MPS) for c...
What is the current status of trial NCT03026257?
This trial is currently completed. It is a NA study. The enrollment target is 323 participants. The study started on 2017-02-13. Estimated completion is 2017-08-18.
What conditions does trial NCT03026257 study?
This clinical trial studies the following conditions: Myopia, Refractive Errors, Hypermetropia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03026257?
The interventions under investigation include: Lotrafilcon B contact lenses with added wetting agent (DEVICE), Samfilcon A contact lenses (DEVICE), POLYQUAD/ALDOX-preserved contact lens solution with added wetting agent (DEVICE), Hydrogen peroxide-based contact lens solution with added wetting agent (DEVICE), Senofilcon C contact lenses (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03026257?
This trial is sponsored by Alcon, a Novartis Company, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03026257 being conducted?
This trial has 8 study locations across Alabama, Ohio, Tennessee, Texas, Ontario. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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