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NCT05805150 · ClinicalTrials.gov registry record · NA
Performance Evaluation of Daily Disposable Contact Lenses in Habitual Lens Wearers Who Use Digital Devices Frequently
A NA study of Myopia, sponsored by CooperVision.
- Completed
- Registry status
- NA
- Development phase
- 69
- Enrollment target
- 4
- Study locations
NCT05805150 is a NA study of Myopia that has completed, run by CooperVision. The registered enrollment target is 69 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (74% lower). The trial reports 4 study locations across 4 states.
The verdict
NCT05805150, a NA study of Myopia, has completed, sponsored by CooperVision.
- COMPLETED
- Registry status
- NA
- Development phase
- 69 participants
- Enrollment target
- 4
- Study locations
Study Summary
The goal of this study is to compare the performance of two daily disposable silicone hydrogel lenses.
Conditions Studied
Interventions
- DEVICE Control Lens (stenfilcon A)
- DEVICE Test Lens (senofilcon A)
Study Locations (4)
Kansas
- Kannarr Eye Care - Pittsburg
Minnesota
- Complete Eye Care of Medina - Medina
Pennsylvania
- Nittany Eye Associates - State College
Rhode Island
- West Bay Eye Associates - Warwick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 69 participants |
| Start Date | 2023-03-13 |
| Est. Completion | 2023-06-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05805150
The ClinicalTrials.gov registry entry for NCT05805150 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 69 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (74% lower). 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 2 interventions - of which Control Lens (stenfilcon A) is the first listed.
NCT05805150 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Kansas, Minnesota, Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT05805150 about?
NCT05805150 is a clinical study titled "Performance Evaluation of Daily Disposable Contact Lenses in Habitual Lens Wearers Who Use Digital Devices Frequently". The goal of this study is to compare the performance of two daily disposable silicone hydrogel lenses.
What is the current status of trial NCT05805150?
This trial is currently completed. It is a NA study. The enrollment target is 69 participants. The study started on 2023-03-13. Estimated completion is 2023-06-01.
What conditions does trial NCT05805150 study?
This clinical trial studies the following conditions: Myopia.
What interventions are being tested in trial NCT05805150?
The interventions under investigation include: Control Lens (stenfilcon A) (DEVICE), Test Lens (senofilcon A) (DEVICE).
Who is sponsoring clinical trial NCT05805150?
This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05805150 being conducted?
This trial has 4 study locations across Kansas, Minnesota, Pennsylvania, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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