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COMPLETED NA

Clinical Study of Approved and Investigational Contact Lenses

NCT02708524 · View on ClinicalTrials.gov ↗

Study Summary

This is a multi-site, 5-visit, double-masked, dispensing study comparing an investigational contact lens with currently-marketed contact lenses. The objective of the study is to evaluate the comfort of the lenses when worn for 30 (-2/+6) days on daily wear modality.

Conditions Studied

Interventions

  • DEVICE Senofilcon C Contact Lens
  • DEVICE Comfilcon A Contact Lens
  • DEVICE Lotrafilcon B Contact Lens
  • DEVICE Samfilcon A Contact Lens

Study Locations (18)

Florida

  • — Fruit Cove
  • — Jacksonville
  • — Jacksonville
  • — Longwood
  • — Tallahassee
  • — Tampa

Alabama

  • — Montgomery

Georgia

  • — Roswell

Illinois

  • — Bloomington

Michigan

  • — East Lansing

Minnesota

  • — Medina

New Jersey

  • — Closter

New York

  • — Vestal

Trial Details

FieldValue
Enrollment Target 554 participants
Start Date 2016-01
Est. Completion 2016-03
Phase NA

Sponsor

Johnson & Johnson Vision Care

36 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02708524

The ClinicalTrials.gov registry entry for NCT02708524 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 554 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Vision Care, which has 36 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 Visual Acuity appearing as the primary indexed condition, and to 4 interventions — of which Senofilcon C Contact 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: NCT02708524 reports 18 study locations spanning 13 distinct geographic areas — top geographies include Florida, Alabama, Georgia. 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 NCT02708524 about?

NCT02708524 is a clinical study titled "Clinical Study of Approved and Investigational Contact Lenses". This is a multi-site, 5-visit, double-masked, dispensing study comparing an investigational contact lens with currently-marketed contact lenses. The objective of the study is to evaluate the comfort of the lenses when worn for 30 (-2/+6) days on daily wear modality.

What is the current status of trial NCT02708524?

This trial is currently completed. It is a NA study. The enrollment target is 554 participants. The study started on 2016-01. Estimated completion is 2016-03.

What conditions does trial NCT02708524 study?

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

What interventions are being tested in trial NCT02708524?

The interventions under investigation include: Senofilcon C Contact Lens (DEVICE), Comfilcon A Contact Lens (DEVICE), Lotrafilcon B Contact Lens (DEVICE), Samfilcon A Contact Lens (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02708524?

This trial is sponsored by Johnson & Johnson Vision Care, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02708524 being conducted?

This trial has 18 study locations across Alabama, Florida, Georgia, Illinois, Michigan. 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