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Comparison of Vitreous Levels of Acular LS 0.04%, Xibrom 0.09%, and Nevanac 0.1%
This study has been completed.
Sponsored by: Innovative Medical
Information provided by: Innovative Medical
ClinicalTrials.gov Identifier: NCT00377546
  Purpose

To compare the penetration of three different NSAIDs.


Condition Intervention Phase
Vitrectomy
Drug: Nepafenac
Drug: Ketorolac LS, Bromfenac
Phase IV

Drug Information available for: Ketorolac Ketorolac tromethamine Bromfenac Bromfenac sodium Nepafenac
U.S. FDA Resources
Study Type: Interventional
Study Design: Randomized, Double-Blind, Active Control, Parallel Assignment
  Eligibility

Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Males or females scheduled to undergo Vitrectomy surgery
  • Likely to complete all study visits and able to provide informed consent
  • Visual potential of 20/25 or better

Exclusion Criteria:

  • Known contraindications to any study medication or ingredients
  • Active ocular diseases or uncontrolled systemic disease
  • Active ocular allergies
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00377546

Locations
United States, Massachusetts
Ophthalmic Consultants of Boston
Boston, Massachusetts, United States, 02114
Sponsors and Collaborators
Innovative Medical
Investigators
Principal Investigator: Jeffrey Heier, MD Ophthalmic Consultants of Boston
  More Information

Study ID Numbers: 5264
Study First Received: September 14, 2006
Last Updated: September 23, 2008
ClinicalTrials.gov Identifier: NCT00377546  
Health Authority: United States: Institutional Review Board

Keywords provided by Innovative Medical:
Retinal Surgery

Study placed in the following topic categories:
Bromfenac
Ketorolac
Ketorolac Tromethamine

ClinicalTrials.gov processed this record on January 15, 2009