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Trial · NCT00524264

A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With Cataract Surgery

NCT00524264, Phase 3, Completed, Allergan; results first posted 2009-10-01

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With Cataract Surgery. Trials, record NCT00524264. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00524264

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With Cataract Surgery
NCT number
NCT00524264
Status
Completed
Phases
Phase 3
Enrollment
248 participants, actual
Lead sponsor
Allergan
Conditions
Cataract Extraction, Pain, Inflammation
Interventions
ketorolac
First posted
2007-09-03
Last updated
2009-10-01
Results first posted
2009-10-01

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryResolution of Post Operative InflammationDay 14Anterior chamber inflammation is the sum of biomicroscopic cell and flare; each measured on a scale of 0-4 (Flare: 0 = no flare, 4 = intense flare / Cell: 0 = no cells, 4 = \>50 cells)
SecondaryOcular PainDay 1Measured on a scale of 0-4 (0 = none, 4 = intolerable)
SecondaryMean Pupil AreaDay 0Pupil area post-irrigation and aspiration

Outcomes4

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYResolution of Post Operative InflammationDay 14Modified Intent-to-Treat Population% of participants with a score of 0NUMBER
SECONDARYOcular PainDay 1Modified Intent-to-Treat Population% of participants with a score of 0NUMBER
SECONDARYMean Pupil AreaDay 0Modified Intent-to-Treat Populationmillimeters squared (mm²)MEAN
POST_HOCVisual AcuityChange from baseline at Day 14Modified Intent-to-Treat PopulationPercentage of patients with ≥ 3 linesNUMBER

Results by group8

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Resolution of Post Operative InflammationKetorolac Solution46.3% of participants with a score of 0
Resolution of Post Operative InflammationVehicle Solution25.6% of participants with a score of 0
Ocular PainKetorolac Solution75.0% of participants with a score of 0
Ocular PainVehicle Solution41.0% of participants with a score of 0
Mean Pupil AreaKetorolac Solution41.8Standard Deviation 12.6millimeters squared (mm²)
Mean Pupil AreaVehicle Solution41.1Standard Deviation 14.0millimeters squared (mm²)
Visual AcuityKetorolac Solution59.5Percentage of patients with ≥ 3 lines
Visual AcuityVehicle Solution46.2Percentage of patients with ≥ 3 lines

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDKetorolac Solution164
Overall StudySTARTEDVehicle Solution84
Overall StudyCOMPLETEDKetorolac Solution144
Overall StudyCOMPLETEDVehicle Solution57
Overall StudyNOT COMPLETEDKetorolac Solution20
Overall StudyNOT COMPLETEDVehicle Solution27

Adverse events22

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherForeign body sensation in eyesEye disordersKetorolac Solution8157
otherForeign body sensation in eyesEye disordersVehicle Solution581
otherIritisEye disordersKetorolac Solution8157
otherIritisEye disordersVehicle Solution581
otherEye PainEye disordersKetorolac Solution7157
otherEye PainEye disordersVehicle Solution1581
otherConjunctival HyperemiaEye disordersKetorolac Solution3157
otherConjunctival HyperemiaEye disordersVehicle Solution1281
otherPhotophobiaEye disordersKetorolac Solution2157
otherPhotophobiaEye disordersVehicle Solution881

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityKetorolac Solution
Total, all-cause mortalityVehicle Solution
Total, other adverse eventsKetorolac Solution46
Total, other adverse eventsVehicle Solution52
Total, serious adverse eventsKetorolac Solution2
Total, serious adverse eventsVehicle Solution1

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
21145532DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00524264

GET https://conductscience.org/api/trials/v1/NCT00524264/events?page=2