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NCT00725530 · ClinicalTrials.gov registry record · NA

Evaluation of Deposits on Contact Lenses Worn Extended Wear

A NA study, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
54
Enrollment target

NCT00725530: Completed NA study, sponsored by Alcon Research.

NCT00725530 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 54 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

NCT00725530, a NA study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
NA
Development phase
54 participants
Enrollment target

Study Summary

The purpose of this study was to measure lipid deposits on commercially marketed contact lenses when worn on an extended wear (overnight) basis for 7 days.

Primary Outcome

Film and discrete deposits were assessed with a slit-lamp after 2-5 hours of open eye 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, cl

Interventions

  • DEVICE balafilcon A contact lens (PureVision)
  • DEVICE etafilcon A contact lens (Acuvue2)

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2008-03
Est. Completion 2008-10
Phase NA
Alcon Research

275 total trials

What the finished NCT00725530 record still lists

NCT00725530 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 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 lens (PureVision) is the first listed.

NCT00725530 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00725530 about?

NCT00725530 is a clinical study titled "Evaluation of Deposits on Contact Lenses Worn Extended Wear". The purpose of this study was to measure lipid deposits on commercially marketed contact lenses when worn on an extended wear (overnight) basis for 7 days.

What is the current status of trial NCT00725530?

This trial is currently completed. It is a NA study. The enrollment target is 54 participants. The study started on 2008-03. Estimated completion is 2008-10.

What interventions are being tested in trial NCT00725530?

The interventions under investigation include: balafilcon A contact lens (PureVision) (DEVICE), etafilcon A contact lens (Acuvue2) (DEVICE).

Who is sponsoring clinical trial NCT00725530?

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 NCT00725530's enrollment target sits among peer trials

54 1268th of 2000 higher than 730 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 NCT00725530, the US trial registry maintained by the National Library of Medicine. NCT00725530 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.