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Evaluation of Contact Lens Saline Solutions With Scleral GP Contact Lens Wearers Experiencing Fogging

NCT03525704 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2021-01-27

No results posted yet for this study

Summary

Evaluation of saline solutions used with scleral rigid gas permeable contact lens wearers experiencing debris in the post lens tear reservoir

Conditions

  • Contact Lens Complication
  • Debris in Post Lens Tear Reservoir

Interventions

DEVICE

Saline Solution Enriched

Sterile single dose, Preservative Free, PH Balanced, Enriched with IONs rinsing and Insertion Solution

DEVICE

Saline Rinse Solution

sterile unit dose non-preserved, 0.9% NaCl (normal saline) solution i

Sponsors & Collaborators

  • Andre Vision and Device Research

    collaborator UNKNOWN

  • The Contact Lens Center at Optique

    collaborator UNKNOWN

  • Premiere Vision Group

    collaborator UNKNOWN

  • Havasu Eye Center

    collaborator UNKNOWN

  • Contamac Ltd

    lead INDUSTRY

Principal Investigators

  • Bret Andre, MS, ABOe · AVD Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-09
Primary Completion
2018-12-15
Completion
2018-12-15
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03525704 on ClinicalTrials.gov