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Short-term Study of Two Soft Contact Lenses in Wearers With Low Astigmatism

NCT06873048 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2026-04-08

No results posted yet for this study

Summary

The primary objective of the study is to evaluate and compare the performance of two soft contact lens.

Conditions

  • Astigmatism
  • Myopia
  • Hyperopia

Interventions

DEVICE

Control Contact Lens (stenfilcon A Sphere)

One week of wear

DEVICE

Test Contact Lens (stenfilcon A Toric)

One week of wear

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision International Limited (CVIL)

    lead INDUSTRY

Principal Investigators

  • Lyndon Jones, PhD,FCOptom · Centre for Ocular Research and Education

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Max Age
42 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-26
Primary Completion
2025-07-11
Completion
2025-07-11
FDA Device
Yes

Countries

  • Canada

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 NCT06873048 on ClinicalTrials.gov