Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01015768 · ClinicalTrials.gov registry record · NA

Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear

A NA study, sponsored by Southern California College of Optometry at Marshall B. Ketchum University.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT01015768 is a NA study that has completed, run by Southern California College of Optometry at Marshall B. Ketchum University. The registered enrollment target is 30 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01015768, a NA study, has completed, sponsored by Southern California College of Optometry at Marshall B. Ketchum University.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The purpose of this study is to assess corneal staining and to measure the relative corneal epithelial "barrier" function (the degree to which the cornea can prevent penetration of colored sodium fluorescein dye into the eye) after 8 hours of wear with a known soft contact lens and multipurpose lens care solution combination.

Interventions

  • DEVICE Control
  • DEVICE ReNu Multiplus multipurpose disinfecting solution

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-10
Est. Completion 2010-01
Phase NA

What the Registry Record Tells You About NCT01015768

The ClinicalTrials.gov registry entry for NCT01015768 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Southern California College of Optometry at Marshall B. Ketchum University, which has 18 total studies on file at ClinicalTrials.gov.

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

NCT01015768 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01015768 about?

NCT01015768 is a clinical study titled "Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear". The purpose of this study is to assess corneal staining and to measure the relative corneal epithelial "barrier" function (the degree to which the cornea can prevent penetration of colored sodium fluorescein dye into the eye) after 8 hours of wear with a known soft contact lens and multipurpose lens...

What is the current status of trial NCT01015768?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2009-10. Estimated completion is 2010-01.

What interventions are being tested in trial NCT01015768?

The interventions under investigation include: Control (DEVICE), ReNu Multiplus multipurpose disinfecting solution (DEVICE).

Who is sponsoring clinical trial NCT01015768?

This trial is sponsored by Southern California College of Optometry at Marshall B. Ketchum University, which has 18 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.