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Biomarker Discovery in Two Daily Disposable Contact Lenses

NCT03440242 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 43

Last updated 2018-11-14

No results posted yet for this study

Summary

This is a non-masked, non-randomized, stratified, 4-arm parallel group, non-interventional study where subjects will be enrolled into one of four arms based on their habitual contact lenses. Subjects will be wearing their habitual contact lenses throughout the study and will be scheduled for morning and afternoon visits totaling 10 visits with a \~4-week washout period between visits 6 and 7.

Conditions

  • Visual Acuity

Interventions

DEVICE

JJVC Contact Lens

etafilcon A with PVP DD

DEVICE

Marketed Contact Lens

nelfilcon A DD

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2018-01-09
Primary Completion
2018-10-12
Completion
2018-10-12
FDA Device
Yes

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 NCT03440242 on ClinicalTrials.gov