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Study identifier: NCT06539637 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Ketorolac Levels in Vitreous and Aqueous Samples From Patients Undergoing Combined Cataract and Pars Plana Vitrectomy Surgeries With and Without Intracameral Phenylephrine 1.0% / Ketorolac 0.3%

Condition: Cataract  ·  Sponsor: DHS Consulting

PhaseEARLY_Phase 1
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a clinical trial evaluating Ketorolac levels in vitreous and aqueous humor samples from patients undergoing combined cataract and pars plana vitrectomy surgeries with and without intracameral phenylephrine 1.0% / ketorolac 0.3% (OMIDRIA). Patients not receiving intracameral OMIDRIA will receive topical ketorolac prior to cataract surgery/pars plana vitrectomy.

This description comes directly from the study's public registry record.

Talk to the study team

Eric Donnenfeld, MD  ·  516 804 5200  ·  ericdonnenfeld@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ophthalmic Consultants of Long IslandWestbury, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06539637