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The Effect of Tear Supplements on Contact Lens Comfort

NCT02956083 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-11-04

No results posted yet for this study

Summary

The primary goal of this investigation is to determine if lipid based artificial tear supplementation has an impact on contact lens discomfort (CLD).

Conditions

  • Dry Eye Syndromes
  • Meibomian Gland Dysfunction

Interventions

OTHER

Systane Balance eye drops

Propylene Glycol 0.6% Over the counter lipid based artificial tears.

OTHER

Systane Contacts eye drops

Hydroxypropyl methycellulose over the counter non-lipid based artificial tears

OTHER

saline

Saline - no brand name

Sponsors & Collaborators

  • University of the Incarnate Word

    lead OTHER

Principal Investigators

  • Srihari Narayanan, OD, PhD · University of the Incarnate Word

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2015-07-31
Completion
2015-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02956083 on ClinicalTrials.gov