MedTrace Logo

Clinical Performance of Habitual Wearers of Bioclear 1-day Lenses When Refitted With Biomedics 1-day Extra for 1 Week

NCT02406495 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2020-07-29

Study results available
· View outcomes & findings →

Summary

Open label, 1-week daily disposable, dispensing study

Conditions

  • Myopia
  • Hyperopia

Interventions

DEVICE

filcon IV 1

contact lens

DEVICE

ocufilcon D

contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Robert Montés-Mico, OD MPhil PhD · Optometry Research Group (GIO) Optics Department, University of Valencia

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2015-04-30
Completion
2015-05-31

Countries

  • Spain

Study Locations

More Related Trials

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 NCT02406495 on ClinicalTrials.gov