Actively Recruiting

Early Phase 1
Age: 18Years +
All Genders
NCT06539637

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%

Led by DHS Consulting · Updated on 2024-08-06

20

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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%

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to provide informed consent
  • Undergoing cataract surgery immediately followed by pars plana vitrectomy
  • Diagnosed preoperatively with a structural pathology requiring vitrectomy (e.g., epiretinal membrane, macular hole, and symptomatic vitreous floaters)
  • Willing and able to comply with all study procedures
  • Male or female, aged 9 18 years
Not Eligible

You will not qualify if you...

  • Age < 18
  • Participating in another clinical trial
  • Patients undergoing cataract surgery or pars plana vitrectomy alone (not a combined procedure)
  • Previous vitrectomy
  • Complications at the time of cataract surgery
  • A tear in the posterior capsule

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ophthalmic Consultants of Long Island

Westbury, New York, United States, 11590

Actively Recruiting

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Research Team

E

Eric Donnenfeld, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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