MedTrace Logo

A Clinical Assessment of the Hemacopolymer Daily Disposable Limbal Ring Soft Contact Lens

NCT01965262 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2017-03-16

Study results available
· View outcomes & findings →

Summary

This purpose of this study is to compare the clinical performance and subjective acceptance of two different daily disposable limbal ring lenses.

Conditions

  • Myopia

Interventions

DEVICE

Hema-copolymer Lens

contact lens

DEVICE

etafilcon A Lens

contact lens

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Carole Maldonado-Codinal, PhD · Eurolens Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2014-05-31
Completion
2014-10-31

Countries

  • United Kingdom

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 NCT01965262 on ClinicalTrials.gov