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A Clinical Comparison of Two Soft Multifocal Contact Lenses

NCT05794126 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2024-04-10

Study results available
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Summary

The study objective was to gather short-term clinical performance data for two soft multifocal contact lenses.

Conditions

Interventions

DEVICE

Lens 1

Soft multifocal hydrogel contact lens for 15 minutes

DEVICE

Lens 2

Soft multifocal silicone hydrogel contact lens for 15 minutes.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Philip Morgan, PhD, MCOptom · Eurolens Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
42 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2023-03-23
Completion
2023-03-23
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT05794126 on ClinicalTrials.gov