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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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01254747
The ClinicalTrials.gov registry entry for NCT01254747 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). The listed sponsor is Ciba Vision, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Delefilcon A contact lens is the first listed.
NCT01254747 reports 0 study locations.
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.
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