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NCT01464255 · ClinicalTrials.gov registry record · NA

Comparative Study of Two Marketed 1-day Soft Contact Lenses

A NA study, sponsored by CooperVision.

Completed
Registry status
NA
Development phase
71
Enrollment target

NCT01464255: Completed NA study, sponsored by CooperVision.

NCT01464255 is a NA study that has completed, run by CooperVision. The registered enrollment target is 71 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01464255, a NA study, has completed, sponsored by CooperVision.

COMPLETED
Registry status
NA
Development phase
71 participants
Enrollment target

Study Summary

This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

Primary Outcome

The ophthalmologist's objective assessment of lens fit measurement of decentration after insertion (20 minutes settling) of Pair #1 (measured at baseline visit) and Pair #2 (measured at 7 days after baseline visit). (mm, horizontal and vertical).

Interventions

  • DEVICE ocufilcon D
  • DEVICE ocufilcon B

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2011-08
Est. Completion 2011-11
Phase NA
CooperVision

64 total trials

What the finished NCT01464255 record still lists

NCT01464255 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which ocufilcon D is the first listed.

NCT01464255 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01464255 about?

NCT01464255 is a clinical study titled "Comparative Study of Two Marketed 1-day Soft Contact Lenses". This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

What is the current status of trial NCT01464255?

This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2011-08. Estimated completion is 2011-11.

What interventions are being tested in trial NCT01464255?

The interventions under investigation include: ocufilcon D (DEVICE), ocufilcon B (DEVICE).

Who is sponsoring clinical trial NCT01464255?

This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01464255's enrollment target sits among peer trials

71 1102nd of 2000 higher than 898 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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Source: ClinicalTrials.gov NCT01464255, the US trial registry maintained by the National Library of Medicine. NCT01464255 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.