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COMPLETED NA

Lens Wearing Experience and Biocompatibility of a Multi-Purpose Disinfecting Solution (MPDS)

NCT01476722 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study was to evaluate the efficacy of a new multipurpose disinfecting solution in silicone hydrogel and soft contact lens wearers.

Conditions Studied

Interventions

  • DEVICE OPTI-FREE PureMoist multipurpose disinfecting solution

Study Locations (1)

Texas

  • Contact Alcon Call Center for Trial Locations — Fort Worth

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2011-06
Est. Completion 2011-10
Phase NA

Sponsor

Alcon Research

111 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01476722

The ClinicalTrials.gov registry entry for NCT01476722 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 125 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 111 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 1 intervention — of which OPTI-FREE PureMoist multipurpose disinfecting solution 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: NCT01476722 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. 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 NCT01476722 about?

NCT01476722 is a clinical study titled "Lens Wearing Experience and Biocompatibility of a Multi-Purpose Disinfecting Solution (MPDS)". The purpose of this study was to evaluate the efficacy of a new multipurpose disinfecting solution in silicone hydrogel and soft contact lens wearers.

What is the current status of trial NCT01476722?

This trial is currently completed. It is a NA study. The enrollment target is 125 participants. The study started on 2011-06. Estimated completion is 2011-10.

What conditions does trial NCT01476722 study?

This clinical trial studies the following conditions: Healthy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01476722?

The interventions under investigation include: OPTI-FREE PureMoist multipurpose disinfecting solution (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01476722?

This trial is sponsored by Alcon Research, which has 111 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01476722 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial