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NCT00405431 · ClinicalTrials.gov registry record · NA

Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery?

A NA study, sponsored by Wills Eye.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT00405431: Completed NA study, sponsored by Wills Eye.

NCT00405431 is a NA study that has completed, run by Wills Eye. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00405431, a NA study, has completed, sponsored by Wills Eye.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether reducing inflammation of the surface of the eye with topical Restasis after glaucoma surgery will improve surgical outcomes and increase patient comfort.

Interventions

  • DRUG Restasis
  • DRUG Endura (artificial tears)

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2004-03
Est. Completion 2007-11
Phase NA
Wills Eye

59 total trials

What the finished NCT00405431 record still lists

NCT00405431 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

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

NCT00405431 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00405431 about?

NCT00405431 is a clinical study titled "Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery?". The purpose of this study is to determine whether reducing inflammation of the surface of the eye with topical Restasis after glaucoma surgery will improve surgical outcomes and increase patient comfort.

What is the current status of trial NCT00405431?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2004-03. Estimated completion is 2007-11.

What interventions are being tested in trial NCT00405431?

The interventions under investigation include: Restasis (DRUG), Endura (artificial tears) (DRUG).

Who is sponsoring clinical trial NCT00405431?

This trial is sponsored by Wills Eye, which has 59 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00405431's enrollment target sits among peer trials

43 1435th of 2000 higher than 565 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 NCT00405431, the US trial registry maintained by the National Library of Medicine. NCT00405431 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.