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NCT00725153 · ClinicalTrials.gov registry record · NA

Evaluation of Deposits on Contact Lenses Worn Daily Wear

A NA study, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
55
Enrollment target

NCT00725153: Completed NA study, sponsored by Alcon Research.

NCT00725153 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 55 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00725153, a NA study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
NA
Development phase
55 participants
Enrollment target

Study Summary

The purpose of this study was to measure front surface deposits on contact lenses when worn for ten hours.

Primary Outcome

Film and discrete deposits were assessed with a slit-lamp after 10 hours of lens wear. Film deposits were recorded on a 5-point scale, where 0=no deposition, clean surface; 1=slight, deposition occupying 1-5% of lens front surface; 2=mild, deposition occupying 6-15% of lens front surface; 3=moderate, deposition occupying 16-25% of lens front surface; 4=severe, deposition occupying \>25% of lens front surface. Discrete deposits were recorded on a 5-point scale, where 0=no deposition, clean surfac

Interventions

  • DEVICE Balafilcon A contact lenses (PureVision)
  • DEVICE Etafilcon A contact lenses (Acuvue2)

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2008-03
Est. Completion 2008-09
Phase NA
Alcon Research

275 total trials

What the finished NCT00725153 record still lists

NCT00725153 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Balafilcon A contact lenses (PureVision) is the first listed.

NCT00725153 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00725153 about?

NCT00725153 is a clinical study titled "Evaluation of Deposits on Contact Lenses Worn Daily Wear". The purpose of this study was to measure front surface deposits on contact lenses when worn for ten hours.

What is the current status of trial NCT00725153?

This trial is currently completed. It is a NA study. The enrollment target is 55 participants. The study started on 2008-03. Estimated completion is 2008-09.

What interventions are being tested in trial NCT00725153?

The interventions under investigation include: Balafilcon A contact lenses (PureVision) (DEVICE), Etafilcon A contact lenses (Acuvue2) (DEVICE).

Who is sponsoring clinical trial NCT00725153?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00725153's enrollment target sits among peer trials

55 1264th of 2000 higher than 733 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 NCT00725153, the US trial registry maintained by the National Library of Medicine. NCT00725153 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.