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Topical 0.4% Ketorolac and Vitreoretinal Surgery | Clinical Trials | Clareo Health

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COMPLETEDPhase 2/3NCT00576329

Topical 0.4% Ketorolac and Vitreoretinal Surgery

To determine whether use of topical 0.4% ketorolac has any effect on pupil size during vitreoretinal surgery.

Lead sponsor: Emory University•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Emory University

Other outcomes will be to assess postoperative pain and inflammation and visual acuity.

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Age of 18, routine elective vitrectomy

Exclusion Criteria

•history of trauma, uveitis, prior intraocular surgery within 3 months, requirement of mechanical pupil dilation, prior inclusion of other eye

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: May 14, 2014Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE2/PHASE3

Enrollment76

Start dateNov 2006

Last updatedMay 14, 2014

Condition

Locations shown

Emory Eye Clinic

Atlanta, Georgia

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 14, 2014Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions