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NCT01475877 · ClinicalTrials.gov registry record

Bromday Versus Nevanac Eye Drops to Control Pain Following Photorefractive Keratectomy

A clinical trial of Myopia, sponsored by Virdi Eye Clinic.

Completed
Registry status
20
Enrollment target
1
Study location

NCT01475877: Completed study of Myopia, sponsored by Virdi Eye Clinic.

NCT01475877 is a study of Myopia that has completed, run by Virdi Eye Clinic. The registered enrollment target is 20 participants, below the 268-participant average among 90 other Myopia trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01475877, a study of Myopia, has completed, sponsored by Virdi Eye Clinic.

COMPLETED
Registry status
20 participants
Enrollment target
1
Study location

Study Summary

This study will compare the effect of two topical non-steroidal antiinflammatory agents to control pain after photorefractive keratectomy (PRK) eye surgery.

Conditions Studied

Interventions

  • DRUG Bromfenac

Study Locations (1)

Illinois

  • Virdi Eye Clinic and Laser Vision Center - Rock Island

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2011-05
Est. Completion 2012-05
Virdi Eye Clinic

1 total trials

What the finished NCT01475877 record still lists

NCT01475877 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 268-participant average among 90 other Myopia trials with a reported enrollment target (93% lower).

The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which Bromfenac is the first listed.

NCT01475877 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT01475877 about?

NCT01475877 is a clinical study titled "Bromday Versus Nevanac Eye Drops to Control Pain Following Photorefractive Keratectomy". This study will compare the effect of two topical non-steroidal antiinflammatory agents to control pain after photorefractive keratectomy (PRK) eye surgery.

What is the current status of trial NCT01475877?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2011-05. Estimated completion is 2012-05.

What conditions does trial NCT01475877 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT01475877?

The interventions under investigation include: Bromfenac (DRUG).

Who is sponsoring clinical trial NCT01475877?

This trial is sponsored by Virdi Eye Clinic, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01475877 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Myopia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01475877's enrollment target sits among peer trials

20 88th of 90 higher than 2 of 90 other Myopia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Myopia 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 NCT01475877, the US trial registry maintained by the National Library of Medicine. NCT01475877 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.