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NCT05285527 · ClinicalTrials.gov registry record · NA

MiSight 1 Day Safety Post-Approval Study

A NA study of Myopia, sponsored by CooperVision.

Recruiting
Registry status
NA
Development phase
2,400
Enrollment target
20
Study locations

NCT05285527 is a NA study of Myopia that is actively recruiting participants, run by CooperVision. The registered enrollment target is 2,400 participants, above the 241-participant average among 90 other Myopia trials with a reported enrollment target (896% higher). The trial reports 20 study locations across 7 states.

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The verdict

NCT05285527, a NA study of Myopia, is actively recruiting participants, sponsored by CooperVision.

RECRUITING
Registry status
NA
Development phase
2,400 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this post-approval study is to confirm the safety of daily disposable soft contact lens wear among the intended patient population for the MiSight 1 Day lens in the US.

Conditions Studied

Myopia

Interventions

  • DEVICE MiSight 1 Day

Study Locations (20)

California

  • University of California, Berkeley University Eye Center - Berkeley
  • Golden Vision Cupertino Optometry - Cupertino
  • Boghossian Vision - Danville
  • Iron Horse Optometric Group - Dublin
  • Capitol Eye Care Center Optometry - Fremont
  • Irvine Eye Physicians and Surgeons Inc - Irvine
  • Elsa Pao OD, Inc - Oakland
  • Perfect Pair Optometry - San Jose
  • Almaden Family Optometric Center - San Jose

Florida

  • Planet Vision Eyecare - Lake Worth
  • Marino Eye Care - Miami
  • Vision Source Oviedo, INC - Oviedo
  • Dau Family Eye Care - Saint Johns
  • Gulf Coast Eye Center - Sarasota
  • Weston Contact Lens Institute LLC - Weston

Arizona

  • Experts on Sight LLC. - Gilbert

Arkansas

  • Centerton Family Eyecare - Centerton

Colorado

  • Children's Eye Physicians - Centennial

Connecticut

  • Eye Physicians & Surgeons, PC - Milford

Illinois

  • Lurie Childrens - Chicago

Trial Details

FieldValue
Enrollment Target 2,400 participants
Start Date 2022-08-15
Est. Completion 2027-05-30
Phase NA

Sponsor

CooperVision

64 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05285527

The ClinicalTrials.gov registry entry for NCT05285527 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 2,400 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 241-participant average among 90 other Myopia trials with a reported enrollment target (896% higher). The listed sponsor is CooperVision, which has 64 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which MiSight 1 Day is the first listed.

NCT05285527 reports 20 study locations spanning 7 distinct geographic areas - top geographies include California, Florida, Arizona.

Frequently Asked Questions

What is clinical trial NCT05285527 about?

NCT05285527 is a clinical study titled "MiSight 1 Day Safety Post-Approval Study". The purpose of this post-approval study is to confirm the safety of daily disposable soft contact lens wear among the intended patient population for the MiSight 1 Day lens in the US.

What is the current status of trial NCT05285527?

This trial is currently recruiting. It is a NA study. The enrollment target is 2,400 participants. The study started on 2022-08-15. Estimated completion is 2027-05-30.

What conditions does trial NCT05285527 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT05285527?

The interventions under investigation include: MiSight 1 Day (DEVICE).

Who is sponsoring clinical trial NCT05285527?

This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05285527 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.