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Phase 4 N=126 Randomized Single-blind Treatment

A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%), Xibrom (Bromfenac 0.09%)and Nevanac (Nepafenac)in Patients Undergoing Phacoemulsification

Cataracts

Enrolled (actual)
126
Serious AEs
0.0%
Results posted
Aug 2011
Primary outcome: Primary: Aqueous PGE2 Inhibition — 288.7; 320.4; 224.8 pg/ml

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Ketorolac Tromethamine (Drug); Bromfenac (Drug); nepafenac (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Frank A. Bucci, Jr., M.D.
Primary completion
Dec 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Aqueous PGE2 Inhibition
288.7; 320.4; 224.8

Summary

Approximately 126 subjects scheduled to undergo cataract surgery by phacoemulsification, will be randomized in an even allocation (1:1:1) to either Acuvail, Xibrom or Nevanac. Subjects will be instructed to begin dosing the study medication in the operative eye the day before surgery and continue dosing on the day of surgery. Beginning one hour before surgery 1 drop of study medication will be instilled by operating room staff approximately every 15 minutes for a total of 3 doses. At the designated time a paracentesis will be performed at the start of the cataract procedure and at least 0.15cc of aqueous humor will be collected. The sample will be immediately stored on dry ice and shipped to a laboratory for analysis.

Eligibility Criteria

Inclusion Criteria

  • Subjects must be 18 years of age or older
  • Scheduled for cataract surgery by phacoemulsification
  • Subjects must be willing to comply with all study requirements and be willing to give informed consent

Exclusion Criteria

  • Any subject that has a history of uveitis or active iritis
  • Subject can have o previous eye surgery with the exception of refractive surgery but not within 6 month
  • No ocular use of prostaglandins within 2 weeks of surgery
  • Use of oral, injectable or topical ophthalmic steroids, NSAIDs of immunosuppressants within 14 days prior to surgery
  • Contraindications to nonsteroidal anti-inflammatory drugs (NSAIDs)
  • Active ocular infection
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01021761). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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