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A Clinical Comparison of Proclear® 1 Day Multifocal and Clariti® 1 Day Multifocal 3 Add

NCT06869044 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 67

Last updated 2026-04-13

No results posted yet for this study

Summary

The aim of this study is to compare the overall lens satisfaction between two soft multifocal contact lenses.

Conditions

Interventions

DEVICE

omafilcon A lens

Participants will be randomized to wear omafilcon A lens for 15 minutes.

DEVICE

Low ADD power somofilcon A lens

Participants will be randomized to wear low ADD power somofilcon A lens for 15 minutes.

DEVICE

Medium ADD power somofilcon A lens

Participants will be randomized to wear medium ADD power somofilcon A lens for 15 minutes.

DEVICE

High ADD power somofilcon A lens

Participants will be randomized to wear high ADD power somofilcon A lens for 15 minutes.

Sponsors & Collaborators

Principal Investigators

  • Meng C Lin, OD, Ph.D · UC Berkeley

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-11
Primary Completion
2025-06-26
Completion
2025-06-26
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT06869044 on ClinicalTrials.gov