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NCT03209505 · ClinicalTrials.gov registry record · Phase 4

The Impact of Contact Lens Coefficient of Friction (CoF) on the Development of Lid Wiper Epitheliopathy (LWE)

A Phase 4 study, sponsored by University of Houston.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target

NCT03209505 is a Phase 4 study that has completed, run by University of Houston. The registered enrollment target is 20 participants.

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The verdict

NCT03209505, a Phase 4 study, has completed, sponsored by University of Houston.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target

Study Summary

This study examines the development of Lid Wiper Epitheliopathy (LWE) in individuals fit with contact lenses having difference coefficients of friction (CoF)

Interventions

  • DEVICE Acuvue Oasys
  • DEVICE Air Optix Night & Day Aqua

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2017-06-26
Est. Completion 2018-04-13
Phase Phase 4

Sponsor

University of Houston

64 total trials

What the Registry Record Tells You About NCT03209505

The ClinicalTrials.gov registry entry for NCT03209505 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Houston, which has 64 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Acuvue Oasys is the first listed.

NCT03209505 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03209505 about?

NCT03209505 is a clinical study titled "The Impact of Contact Lens Coefficient of Friction (CoF) on the Development of Lid Wiper Epitheliopathy (LWE)". This study examines the development of Lid Wiper Epitheliopathy (LWE) in individuals fit with contact lenses having difference coefficients of friction (CoF)

What is the current status of trial NCT03209505?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2017-06-26. Estimated completion is 2018-04-13.

What interventions are being tested in trial NCT03209505?

The interventions under investigation include: Acuvue Oasys (DEVICE), Air Optix Night & Day Aqua (DEVICE).

Who is sponsoring clinical trial NCT03209505?

This trial is sponsored by University of Houston, which has 64 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.