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NCT01309100 · ClinicalTrials.gov registry record · NA
Product Feasibility of a New Silicone Hydrogel Contact Lens
A NA study, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- NA
- Development phase
- 144
- Enrollment target
NCT01309100: Completed NA study, sponsored by Bausch & Lomb Incorporated.
NCT01309100 is a NA study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 144 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01309100, a NA study, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- NA
- Development phase
- 144 participants
- Enrollment target
Study Summary
The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lens.
Primary Outcome
The mean difference in distance high contrast logMAR visual acuity(VA) between the investigational lens (RD2117-01) and the Air Optix Aqua control lens.
Interventions
- DEVICE Investigational Lens
- DEVICE Acuvue Oasys Lens
- DEVICE Air Optix Aqua Lens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 144 participants |
| Start Date | 2010-11 |
| Est. Completion | 2011-01 |
| Phase | NA |
What the finished NCT01309100 record still lists
NCT01309100 is an interventional study that assigns participants to a tested intervention. The registered 144 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 3 interventions - of which Investigational Lens is the first listed.
NCT01309100 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01309100 about?
NCT01309100 is a clinical study titled "Product Feasibility of 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 lens.
What is the current status of trial NCT01309100?
This trial is currently completed. It is a NA study. The enrollment target is 144 participants. The study started on 2010-11. Estimated completion is 2011-01.
What interventions are being tested in trial NCT01309100?
The interventions under investigation include: Investigational Lens (DEVICE), Acuvue Oasys Lens (DEVICE), Air Optix Aqua Lens (DEVICE).
Who is sponsoring clinical trial NCT01309100?
This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01309100's enrollment target sits among peer trials
144 706th of 2000 higher than 1,290 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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.
Source ClinicalTrials.gov registry export · 2026-08-08
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