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2-week Evaluation of Marketed Silicone Hydrogel Contact Lenses in Indian Population

NCT02394808 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2018-06-19

Study results available
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Summary

The primary objective of this study is to evaluate the clinical performance of two marketed silicone hydrogel contact lenses in an Indian population in the following areas: physiological characteristics, comfort characteristics and vision characteristics.

Conditions

  • Visual Acuity

Interventions

DEVICE

senofilcon A

One fresh pair of contact lenses worn for 11 (+/-2) days, for a minimum of 6 hours per day

DEVICE

lotrafilcon B

One fresh pair of contact lenses worn for 11 (+/-2) days, for a minimum of 6 hours per day

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-01
Primary Completion
2015-09-01
Completion
2015-09-01

Countries

  • India

Study Locations

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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 NCT02394808 on ClinicalTrials.gov