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NCT01518868 · ClinicalTrials.gov registry record · NA
A Study to Evaluate the Feasibility of a High Add Multi Focal Contact Lens
A NA study, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- NA
- Development phase
- 126
- Enrollment target
NCT01518868: Completed NA study, sponsored by Bausch & Lomb Incorporated.
NCT01518868 is a NA study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 126 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01518868, a NA study, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- NA
- Development phase
- 126 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the product performance of the investigational multifocal high add soft contact lens compared with PureVision Multi-focal contact lens on a daily wear basis.
Primary Outcome
Visual acuity was assessed by distance high contrast logarithm of the minimum angle of resolution (logMAR).
Interventions
- DEVICE Investigational contact lens
- DEVICE PureVision contact lens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 126 participants |
| Start Date | 2012-01 |
| Est. Completion | 2012-02 |
| Phase | NA |
What the finished NCT01518868 record still lists
NCT01518868 is an interventional study that assigns participants to a tested intervention. The registered 126 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 (91% lower).
The record links to 0 conditions, and to 2 interventions - of which Investigational contact lens is the first listed.
NCT01518868 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01518868 about?
NCT01518868 is a clinical study titled "A Study to Evaluate the Feasibility of a High Add Multi Focal Contact Lens". The objective of this study is to evaluate the product performance of the investigational multifocal high add soft contact lens compared with PureVision Multi-focal contact lens on a daily wear basis.
What is the current status of trial NCT01518868?
This trial is currently completed. It is a NA study. The enrollment target is 126 participants. The study started on 2012-01. Estimated completion is 2012-02.
What interventions are being tested in trial NCT01518868?
The interventions under investigation include: Investigational contact lens (DEVICE), PureVision contact lens (DEVICE).
Who is sponsoring clinical trial NCT01518868?
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 NCT01518868's enrollment target sits among peer trials
126 749th of 2000 higher than 1,248 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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