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NCT01254747 · ClinicalTrials.gov registry record · NA
Clinical Evaluation of an Investigational Soft Contact Lens
A NA study, sponsored by Ciba Vision.
- Completed
- Registry status
- NA
- Development phase
- 130
- Enrollment target
NCT01254747: Completed NA study, sponsored by Ciba Vision.
NCT01254747 is a NA study that has completed, run by Ciba Vision. The registered enrollment target is 130 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
NCT01254747, a NA study, has completed, sponsored by Ciba Vision.
- COMPLETED
- Registry status
- NA
- Development phase
- 130 participants
- Enrollment target
Study Summary
The purpose of this 4-week dispensing trial is to evaluate and compare an investigational soft contact lens worn on a daily disposable basis with three other soft contact lenses also worn on a daily disposable basis.
Primary Outcome
Overall comfort was assessed and recorded by the participant on a questionnaire as a single, retrospective evaluation of 4 weeks of wear. Overall comfort was measured on a 10-point scale, with 1 being poor and 10 being excellent.
Interventions
- DEVICE Delefilcon A contact lens
- DEVICE Lotrafilcon B contact lens (O2 OPTIX, AIR OPTIX)
- DEVICE Nelfilcon A contact lens (DAILIES AquaComfort Plus)
- DEVICE Narafilcon A contact lens (1-DAY ACUVUE TRUEYE)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 130 participants |
| Start Date | 2010-11 |
| Est. Completion | 2010-12 |
| Phase | NA |
What the finished NCT01254747 record still lists
NCT01254747 is an interventional study that assigns participants to a tested intervention. The registered 130 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 4 interventions - of which Delefilcon A contact lens is the first listed.
NCT01254747 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01254747 about?
NCT01254747 is a clinical study titled "Clinical Evaluation of an Investigational Soft Contact Lens". The purpose of this 4-week dispensing trial is to evaluate and compare an investigational soft contact lens worn on a daily disposable basis with three other soft contact lenses also worn on a daily disposable basis.
What is the current status of trial NCT01254747?
This trial is currently completed. It is a NA study. The enrollment target is 130 participants. The study started on 2010-11. Estimated completion is 2010-12.
What interventions are being tested in trial NCT01254747?
The interventions under investigation include: Delefilcon A contact lens (DEVICE), Lotrafilcon B contact lens (O2 OPTIX, AIR OPTIX) (DEVICE), Nelfilcon A contact lens (DAILIES AquaComfort Plus) (DEVICE), Narafilcon A contact lens (1-DAY ACUVUE TRUEYE) (DEVICE).
Who is sponsoring clinical trial NCT01254747?
This trial is sponsored by Ciba Vision, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01254747's enrollment target sits among peer trials
130 733rd of 2000 higher than 1,257 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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