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COMPLETED

A Dispensing Clinical Trial of Test Contact Lens Against Marketed Contact Lens

NCT03499067 · View on ClinicalTrials.gov ↗

Study Summary

Evaluation of the clinical performance of an investigational silicone-hydrogel contact lens (test) compared to a marketed lens (control), when worn on a daily basis for 1 month.

Conditions Studied

Interventions

  • DEVICE Test lens
  • DEVICE Control lens

Study Locations (2)

California

  • Clinical Research Center, University of California, Berkeley — Berkeley

Indiana

  • Clinical Optics Research Lab (CORL) Indiana University School of Optometry, Indiana University — Bloomington

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2018-04-11
Est. Completion 2018-08-01

Sponsor

CooperVision

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03499067

The ClinicalTrials.gov registry entry for NCT03499067 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 58 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CooperVision, which has 20 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 Myopia appearing as the primary indexed condition, and to 2 interventions — of which Test lens 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: NCT03499067 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Indiana. 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 NCT03499067 about?

NCT03499067 is a clinical study titled "A Dispensing Clinical Trial of Test Contact Lens Against Marketed Contact Lens". Evaluation of the clinical performance of an investigational silicone-hydrogel contact lens (test) compared to a marketed lens (control), when worn on a daily basis for 1 month.

What is the current status of trial NCT03499067?

This trial is currently completed. The enrollment target is 58 participants. The study started on 2018-04-11. Estimated completion is 2018-08-01.

What conditions does trial NCT03499067 study?

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

What interventions are being tested in trial NCT03499067?

The interventions under investigation include: Test lens (DEVICE), Control lens (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03499067?

This trial is sponsored by CooperVision, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03499067 being conducted?

This trial has 2 study locations across California, Indiana. 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