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NCT04789382 · ClinicalTrials.gov registry record · NA
Three Daily Wear Monthly Replacement Silicone Hydrogel Contact Lenses With Two Multi-purpose Disinfecting Solution Combinations
A NA study of Refractive Errors, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT04789382 is a NA study of Refractive Errors that has completed, run by Alcon Research. The registered enrollment target is 36 participants, below the 104-participant average among 14 other Refractive Errors trials with a reported enrollment target (65% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04789382, a NA study of Refractive Errors, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate corneal staining observed after 2 hours of wear with an investigational contact lens against both PureVision contact lenses pre-cycled with Biotrue and Biofinity contact lenses pre-cycled with RepleniSH.
Conditions Studied
Interventions
- DEVICE LID018869+RepleniSH
- DEVICE LID018869+Biotrue
- DEVICE Biofinity+RepleniSH
- DEVICE PV+Biotrue
Study Locations (1)
Florida
- Alcon Investigator 6565 - Maitland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2021-04-07 |
| Est. Completion | 2021-05-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04789382
The ClinicalTrials.gov registry entry for NCT04789382 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 104-participant average among 14 other Refractive Errors trials with a reported enrollment target (65% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Refractive Errors appearing as the primary indexed condition, and to 4 interventions - of which LID018869+RepleniSH is the first listed.
NCT04789382 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT04789382 about?
NCT04789382 is a clinical study titled "Three Daily Wear Monthly Replacement Silicone Hydrogel Contact Lenses With Two Multi-purpose Disinfecting Solution Combinations". The purpose of this study is to evaluate corneal staining observed after 2 hours of wear with an investigational contact lens against both PureVision contact lenses pre-cycled with Biotrue and Biofinity contact lenses pre-cycled with RepleniSH.
What is the current status of trial NCT04789382?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2021-04-07. Estimated completion is 2021-05-07.
What conditions does trial NCT04789382 study?
This clinical trial studies the following conditions: Refractive Errors.
What interventions are being tested in trial NCT04789382?
The interventions under investigation include: LID018869+RepleniSH (DEVICE), LID018869+Biotrue (DEVICE), Biofinity+RepleniSH (DEVICE), PV+Biotrue (DEVICE).
Who is sponsoring clinical trial NCT04789382?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04789382 being conducted?
This trial has 1 study location across Florida. 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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