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Effect of Prophylactic Ketorolac on CME After Cataract Surgery

Q

Queen's University

Status

Completed

Conditions

Macular Edema, Cystoid

Treatments

Drug: ketorolac tromethamine 0.5% (Acular®)

Study type

Interventional

Funder types

Other

Identifiers

NCT00335439
QUEENS-SRE-2

Details and patient eligibility

About

The study will evaluate the efficacy of prophylactic administration of the topical nonsteroidal anti-inflammatory drug (NSAID) ketorolac tromethamine 0.5% (Acular®) on cystoid macular edema (CME) in patients having undergone cataract surgery. CME is the most frequent cause of decreased vision after uncomplicated cataract surgery and can result in irreversible sight reduction. The investigation will involve a comparison arm and a treatment arm with both sets of patient populations being evaluated for CME with ophthalmologic examinations and optical coherence tomography (OCT) measurements. The objective is to elucidate the role of NSAID drops in preventing CME after cataract surgery.

Enrollment

98 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • First cataract surgery (i.e., first eye).

Exclusion criteria

  • hypersensitivity to the NSAID drug class,
  • pregnancy.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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