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Clinical Evaluation of Two New Silicone Hydrogel Multifocal Products

NCT00909792 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 259

Last updated 2012-06-29

Study results available
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Summary

The objective of this trial is compare the visual performance, ratings, and preference of two multifocal, soft contact lenses.

Conditions

Interventions

DEVICE

Lotrafilcon B

Silicone hydrogel, soft, multifocal contact lens

DEVICE

Senofilcon A

Silicone hydrogel, soft, multifocal contact lens

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2009-06-30
Completion
2009-06-30

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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 NCT00909792 on ClinicalTrials.gov