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Ketorolac vs. Steroid in the Prevention of CME
This study has been completed.
First Received: June 30, 2006   Last Updated: January 15, 2007   History of Changes
Sponsored by: Innovative Medical
Information provided by: Innovative Medical
ClinicalTrials.gov Identifier: NCT00348244
  Purpose

Evaluate if the incidence of sub clinical CME can be significantly reduced by use of peri-operative Acular LS plus Pred Forte when compared with Pred Forte alone in normal cataract patients.


Condition Intervention Phase
Cataract
Drug: Ketorolac, Prednisolone Acetate
Phase IV

Study Type: Interventional
Study Design: Randomized, Single Blind, Active Control, Parallel Assignment
Official Title: A Masked Comparison of Acular LS Plus Steroid Versus Steroid Alone for the Prevention of Macular Leakage in Cataract Patients

Resource links provided by NLM:

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • · Male or female > 18 years of age scheduled to undergo cataract surgery with surgeon expectation of 20/20 BCVA postoperatively

    • Must be in good general health. Patients with systemic diseases will be enrolled only if there are no ocular manifestations of their disease (ie diabetics with normal retinal exams)
    • Ability to provide informed consent and likely to complete all study visits

Exclusion Criteria:

  • · Known contraindication to any study medication or any of their components

    • Uncontrolled systemic disease
    • Required use of ocular medications other than the study medications during the study
    • Abnormal pre-operative OCTs if obtainable
    • Diabetic patients with a history of macular edema or diabetic retinopathy
    • AMD patients with less than a 20/20 surgical outcome expectation, epi-retinal membranes, retinal vein occlusion, or any pre-existing macular disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00348244

Locations
United States, New York
Dr. Wittpenn
Stony Brook, New York, United States, 11790
Sponsors and Collaborators
Innovative Medical
Investigators
Principal Investigator: John Wittpenn, MD Ophthalmic Consultants of Long Island
  More Information

No publications provided by Innovative Medical

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: 5152
Study First Received: June 30, 2006
Last Updated: January 15, 2007
ClinicalTrials.gov Identifier: NCT00348244     History of Changes
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Anti-Inflammatory Agents
Antineoplastic Agents, Hormonal
Methylprednisolone
Hormone Antagonists
Eye Diseases
Cyclooxygenase Inhibitors
Ketorolac
Hormones, Hormone Substitutes, and Hormone Antagonists
Antiemetics
Methylprednisolone acetate
Lens Diseases
Prednisolone acetate
Neuroprotective Agents
Glucocorticoids
Hormones
Analgesics, Non-Narcotic
Cataract
Prednisolone
Anti-Inflammatory Agents, Non-Steroidal
Analgesics
Peripheral Nervous System Agents
Antirheumatic Agents
Ketorolac Tromethamine
Methylprednisolone Hemisuccinate

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Molecular Mechanisms of Pharmacological Action
Methylprednisolone
Antineoplastic Agents
Ketorolac
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Antiemetics
Prednisolone acetate
Lens Diseases
Hormones
Neuroprotective Agents
Sensory System Agents
Therapeutic Uses
Cataract
Anti-Inflammatory Agents, Non-Steroidal
Analgesics
Methylprednisolone Hemisuccinate
Antineoplastic Agents, Hormonal
Eye Diseases
Cyclooxygenase Inhibitors
Gastrointestinal Agents
Methylprednisolone acetate
Enzyme Inhibitors
Glucocorticoids
Protective Agents
Pharmacologic Actions
Analgesics, Non-Narcotic
Autonomic Agents
Prednisolone

ClinicalTrials.gov processed this record on September 11, 2009