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NCT01309893 · ClinicalTrials.gov registry record · NA
A Study to Evaluate a New Silicone Hydrogel Contact Lens
A NA study of Myopia, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- NA
- Development phase
- 66
- Enrollment target
- 1
- Study location
NCT01309893: Completed NA study of Myopia, sponsored by Bausch & Lomb Incorporated.
NCT01309893 is a NA study of Myopia that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 66 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01309893, a NA study of Myopia, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- NA
- Development phase
- 66 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses.
Primary Outcome
Mean difference in distance high contrast logMAR over all lens VAs (visual acuity) from Baseline and 1 Week
Conditions Studied
Interventions
- DEVICE Investigational Lens
- DEVICE Air Optix Aqua lens
Study Locations (1)
New York
- Bausch & Lomb - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2010-12 |
| Est. Completion | 2011-02 |
| Phase | NA |
What the finished NCT01309893 record still lists
NCT01309893 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (75% lower).
The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 2 interventions - of which Investigational Lens is the first listed.
NCT01309893 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT01309893 about?
NCT01309893 is a clinical study titled "A Study to Evaluate a New Silicone Hydrogel Contact Lens". The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses.
What is the current status of trial NCT01309893?
This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2010-12. Estimated completion is 2011-02.
What conditions does trial NCT01309893 study?
This clinical trial studies the following conditions: Myopia.
What interventions are being tested in trial NCT01309893?
The interventions under investigation include: Investigational Lens (DEVICE), Air Optix Aqua lens (DEVICE).
Who is sponsoring clinical trial NCT01309893?
This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01309893 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT01309893's enrollment target sits among peer trials
66 53rd of 90 higher than 35 of 90 other Myopia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Myopia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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