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Apioc Contact Lens Feasibility

NCT03688672 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2022-01-19

No results posted yet for this study

Summary

This clinical trial will document the feasibility of the Apioc lens design by assessing which lens shape parameters yield successful on-eye-fit and movement of the Apioc contact lens design and evaluate the subjectively-reported comfort of the Apioc contact lens design.

Conditions

  • Ametropia
  • Myopia
  • Hyperopia
  • Astigmatism
  • Presbyopia

Interventions

DEVICE

Apioc Contact Lens Design

Novel soft contact lens design.

Sponsors & Collaborators

  • Lentechs, LLC

    lead INDUSTRY

Principal Investigators

  • Heidi Wagner, OD, MS · Ohio State University

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2018-10-01
Primary Completion
2020-10-31
Completion
2020-10-31
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03688672 on ClinicalTrials.gov