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NCT05483127 · ClinicalTrials.gov registry record · NA
Clinical Comparison of Two Daily Disposable Toric Soft Contact Lenses
A NA study, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 153
- Enrollment target
NCT05483127 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 153 participants.
The verdict
NCT05483127, a NA study, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 153 participants
- Enrollment target
Study Summary
The primary purpose of this study is to demonstrate noninferiority in the visual acuity at distance when wearing PRECISION1™ for Astigmatism (P1fA) soft contact lenses compared to another commercially available, soft toric contact lens, MyDay® toric (MDT).
Interventions
- DEVICE Verofilcon A toric soft contact lenses
- DEVICE Stenfilcon A toric soft contact lenses
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 153 participants |
| Start Date | 2022-09-13 |
| Est. Completion | 2022-10-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05483127
The ClinicalTrials.gov registry entry for NCT05483127 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 153 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Verofilcon A toric soft contact lenses is the first listed.
NCT05483127 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05483127 about?
NCT05483127 is a clinical study titled "Clinical Comparison of Two Daily Disposable Toric Soft Contact Lenses". The primary purpose of this study is to demonstrate noninferiority in the visual acuity at distance when wearing PRECISION1™ for Astigmatism (P1fA) soft contact lenses compared to another commercially available, soft toric contact lens, MyDay® toric (MDT).
What is the current status of trial NCT05483127?
This trial is currently completed. It is a NA study. The enrollment target is 153 participants. The study started on 2022-09-13. Estimated completion is 2022-10-31.
What interventions are being tested in trial NCT05483127?
The interventions under investigation include: Verofilcon A toric soft contact lenses (DEVICE), Stenfilcon A toric soft contact lenses (DEVICE).
Who is sponsoring clinical trial NCT05483127?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
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