MedTrace Logo

Accommodative Relief for Uncomfortable Non-Presbyopes

NCT03544216 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2019-02-15

Study results available
· View outcomes & findings →

Summary

This study will determine how multifocal contact lens correction affects symptoms of discomfort and asthenopia in a group of myopic contact lens wearers in the non-presbyopic age range (ages 30-40 years).

Conditions

  • Asthenopia

Interventions

DEVICE

Multifocal Contact Lens

The multifocal contact lens (Bausch + Lomb ULTRA® for Presbyopia) will be worn for two weeks

DEVICE

Single Vision Contact Lens

The single vision contact lens (Bausch + Lomb ULTRA®) will be worn for two weeks

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    collaborator INDUSTRY

  • Ohio State University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
30 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-02
Primary Completion
2018-05-06
Completion
2018-05-06
FDA Device
Yes

Countries

  • United States

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 NCT03544216 on ClinicalTrials.gov