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Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

NCT02258139 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2020-09-14

Study results available
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Summary

This will be a randomized non-dispensing study comparing the overnight corneal swelling of an eye while wearing no contact lens to the Ultra contract lens.

Conditions

  • Corneal Deformity

Interventions

DEVICE

B&L Investigational Contact Lens

The lens used in this study will be supplied by the Sponsor. All subjects will wear a -3.00D lens.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Robert Steffen, OD, MS · Bausch & Lomb Incorporated

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2014-11-03
Primary Completion
2014-12-11
Completion
2014-12-11

Countries

  • United States

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 NCT02258139 on ClinicalTrials.gov