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NCT00711347 · ClinicalTrials.gov registry record · Phase 4

Intraoperative Floppy Iris Syndrome

A Phase 4 study, sponsored by Alcon Research.

Completed
Registry status
Phase 4
Development phase
28
Enrollment target

NCT00711347: Completed Phase 4 study, sponsored by Alcon Research.

NCT00711347 is a Phase 4 study that has completed, run by Alcon Research. The registered enrollment target is 28 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00711347, a Phase 4 study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
Phase 4
Development phase
28 participants
Enrollment target

Study Summary

An assessment of the surgical performance of DisCoVisc compared to Healon5 during cataract surgery with intraocular lens implantation where miotic/small pupils or intraoperative Floppy Iris Syndrome exists.

Primary Outcome

Endothelial cell loss/gain is measured by comparing the preoperative assessment of endothelial cell density against postoperative measurements. Measurements are made with a specular microscope, which takes a picture and numbers endothelial cells. This endpoint compares the assessment done at 1 month against the assessment done at baseline. A negative number indicates a loss of endothelial cells, a positive number indicates a gain in endothelial cells.

Interventions

  • DEVICE DisCoVisc
  • DEVICE Healon5

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2007-06
Est. Completion 2008-04
Phase Phase 4
Alcon Research

275 total trials

What the finished NCT00711347 record still lists

NCT00711347 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

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

NCT00711347 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00711347 about?

NCT00711347 is a clinical study titled "Intraoperative Floppy Iris Syndrome". An assessment of the surgical performance of DisCoVisc compared to Healon5 during cataract surgery with intraocular lens implantation where miotic/small pupils or intraoperative Floppy Iris Syndrome exists.

What is the current status of trial NCT00711347?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 28 participants. The study started on 2007-06. Estimated completion is 2008-04.

What interventions are being tested in trial NCT00711347?

The interventions under investigation include: DisCoVisc (DEVICE), Healon5 (DEVICE).

Who is sponsoring clinical trial NCT00711347?

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 NCT00711347's enrollment target sits among peer trials

28 1635th of 2000 higher than 350 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT00711347, the US trial registry maintained by the National Library of Medicine. NCT00711347 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.